FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
3M 1154 LASER IMAGER
K Number: K936142
·
Decision Sep 16, 1994
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
120
Applicant Total
3
Review Days
263
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- 3M 1154 LASER IMAGER
- K Number
- K936142
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2040
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- 3M Information,Imaging and Electronic Sector
- Date Received
- December 27, 1993
- Decision Date
- September 16, 1994
- Product Code
- LMC
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LMC | Camera, Multi Format, Radiological | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LMC), ordered by most recent decision date.
SONY DIGITAL PRINTER UP-D898MD/SONY HYBRID PRINTER UP-X898MD
FDA 510(k)
FDA Class 2
·Radiology
SONY HYBIRD GRAPHIC UP-971AD, SONY HYBIRD GRAPHIC PRINTER UP-991AD
FDA 510(k)
FDA Class 2
·Radiology
DRYVIEW CHROMA IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
CYPHER DICOM PRINT SOLUTION
FDA 510(k)
FDA Class 2
·Radiology
CARESTREAM DRYVIEW 5850 LASER IMAGER
FDA 510(k)
FDA Class 2
·Radiology
SONY UP-DF750 DIGITAL FILM IMAGER
FDA 510(k)
FDA Class 2
·Radiology