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: HQB FDA class 2

Photocoagulator And Accessories

Ophthalmic

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A Photocoagulator and Accessories is an ophthalmic surgical device that uses focused light energy, typically from a xenon arc or argon laser source, to thermally coagulate retinal tissue for the treatment of retinal tears, diabetic retinopathy, macular degeneration, and other vascular retinal conditions. This device is FDA Class 2 (moderate risk), requiring premarket notification (510(k)) before marketing. It carries product code HQB and is regulated under 21 CFR 886.4690, within the Ophthalmic medical specialty. It is eligible for third-party review.

510(k) Clearances

30 matches
K Number
Device Name
Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers
MAXReach Laser Probe
Vitreq disposable laser probes, light fibers and Chandelier
PEREGRINE CURVED ILLUMINATING LASER PROBE
23GA CURVED ILLUMINATING LASER PROBE
PEREGRINE 23GA CURVED LASER PROBE
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE
27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA
NIDEK MULTICOLOR SCAN LASER PHOTOCOAGULATOR MC-500 VIXI
NIDEK MULTICOLOR LASER PHOTOCOAGULATOR
LC-250 INFRARED LIGHT COAGULATOR
GAMP & ASSOC. DISPOSABLE ASPIRATING ENDOOCULAR LASER PROBE
GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE
GAMP & ASSOC. DISPOSABLE ILL ENDOCULAR LASER PROBE
OPTOSCALPEL I LASER SYSTEM
THE ENDO OPTIKS MICROPROBE
ZIESS ENDOPROBE
SLT CONTACT LASER SYSTEM CYCLOPHOTOCOAGULATION
SLT CONTACT LASER SYSTEM ENDOPHOTOCOAGULATION
REUSABLE FIBEROPTIC LIGHTPIPE
NIDEK AC-2000 LASER SYSTEM
SYSTEM 930 ARGON PHOTOCOAGULATOR
ARGON/KRYPTON LASER SYSTEM 8500
ARGON LASER PHOTOCOAGULATOR SYS REPEAT MODE
ARGON/KRYPTON & KRYPTON LASER PHOTOCOAGULATION SYS
ARGON/KRYPTON LASER PHOTOCOAGULATOR SYS
SLIT LAMP ATTACHMENT
PHOTOCOAGULATOR LASER
LAMP DELIVERY SYS.-PHOTOCOAGULATION
PHOTOCOAGULATOR, LOG 3 PORTABLE XENON

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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