FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RADIOGRAPHIC FILM PROCESSOR M-30CR &
K Number: K841431
·
Decision Jul 6, 1984
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
3
Review Days
91
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
- RADIOGRAPHIC FILM PROCESSOR M-30CR &
- K Number
- K841431
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1900
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- The Allen Products Co.
- Date Received
- April 6, 1984
- Decision Date
- July 6, 1984
- Product Code
- IXX
- 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 |
|---|---|---|---|
| IXX | Processor, Cine Film | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IXX), ordered by most recent decision date.
JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100
FDA 510(k)
FDA Class 2
·Radiology
AP-6CR CINERADIOGRAPHIC FILM PROCESSOR
FDA 510(k)
FDA Class 2
·Radiology
JAMIESON JT-CRP CINE FILM PROCESSOR
FDA 510(k)
FDA Class 2
·Radiology
STERILE O. R. TOWEL
FDA 510(k)
FDA Class 2
·Radiology
CINE RADIOGRAPHIC FILM PROCESSOR M-45CR
FDA 510(k)
FDA Class 2
·Radiology