Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LMC FDA class 2

Camera, Multi Format, Radiological

Radiology

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Camera, Multi Format, Radiological is a device used to record radiological images in multiple photographic formats onto film from video displays or image intensifiers, used for documentation and archiving of diagnostic images from fluoroscopy, nuclear medicine, or other imaging modalities. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance. The product code is LMC, regulated under 21 CFR 892.2040, within the Radiology medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD
SONY HYBIRD GRAPHIC UP-971AD, SONY HYBIRD GRAPHIC PRINTER UP-991AD
DRYVIEW CHROMA IMAGING SYSTEM
CYPHER DICOM PRINT SOLUTION
CARESTREAM DRYVIEW 5850 LASER IMAGER
SONY UP-DF750 DIGITAL FILM IMAGER
LASER IMAGER DRYPRO MODEL 873
DRYSTAR AXYS, MODEL EYZ4E
DRY LASER IMAGER, DRYPRO MODEL 832
DIGITAL PRINTER P6000D SERIES, MODEL P6000DU
CODONICS HORIZON XL DIGITAL DIRECT LONG FILM IMAGER; CODONICS HORIZON XL-X LONG FILM IMAGER
DRYSTAR MODEL 5500
DRY LASER IMAGER, MODEL DRYPRO MODEL 793
NP-2600 SERIES HARDCOPY PRINTERS
KODAK MEDICAL IMAGER 300
KODAK COLOR MEDICAL IMAGER 1000
KODAK DRYVIEW 8900 LASER IMAGER MAMMOGRAPHY ACCESSORY
FUJI MEDICAL DRY LASER IMAGERS, MODELS DRYPIX 7000, DRYPIX 5000 AND FM-DP L
DRYSTAR 5300 MEDICAL IMAGE PRINTER, MODEL 5300
KONICA LASER IMAGER, MODEL DRYPRO MODEL 771
CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS
UP-DF500 FILMSTATION DIGITAL FILM IMAGER
DRYSTAR 5500
LR DICOM CONTROLLER
CODONICS HORIZON CI MEDICAL MULTIMEDIA DRY IMAGER; CODONICS HORIZON GS MEDICAL MULTIMEDIA GREY SCALE DRY IMAGER
KONICA LASER IMAGER, DRYPRO MODEL 751/752
DRYSTAR, MODEL 4500M
MODIFICATION TO LR 5200 FILM RECORDER
ELK LASER IMAGER, MODEL EL-DRY 4000
LIFEJET PRINTER 400
DRYSTAR 4500 PRINTER, MODEL 4500
CODONICS NP-1660 SERIES MEDICAL PRINTERS, MODEL 1660
KODAK DRYVIEW 8610 LASER IMAGER / FOR MAMMOGRAPHY
KONICA LASER IMAGER, DRYPRO MODEL 722
COLORPOINT 1720 MEDICAL IMAGERS AND VIDEO CAPTURE BOX CX-1000 SERIES
KODAK DIGITAL SCIENCE 3600 DISTRIBUTED MEDICAL IMAGER, KODAK DIGITAL SCIENCE 1200 DISTRIBUTED MEDICAL IMAGER, MODEL 3600
IMATION SE-204 LASER IMAGER
RAVEN DRY PRINTER
LASERSHARE PRINT SPOOLER(2100[SOLARIS X86]/(1500[WINDOWS NT])
HELIOS LASER IMAGER 1417
KODAK DIGITAL SCIENCE 9000D MEDICAL LASER PRINTER (9000D)
COLORPOINT OR PROFESSIONAL COLORPOINT
IMATION SE-196 LASER IMAGER
LR 5200 LASER FILM RECORDER
CODONICS MEDICAL PRINTER (NP-1600M,NP1600MD)
FUJI MEDICAL DRY IMAGER FM-DP 2636
ASPECT OPTICAM
ULTRA COMPACT VIDEO IMAGER
SIENET TELERADIOLOGY PRODUCT LINE
ASPECT DIGITAL FORMATTER

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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