510(k) K963334
- Device
- JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100
- Applicant
- JAMIESON FILM CO.
- 510(k) number
- K963334
- Product code
- IXX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1996-09-11
- Date received
- 1996-08-26
- Regulation
- 892.1900
- Classification name
- Processor, Cine Film
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- GEORGE LEON
- Address
- 10425 Olympic Dr. Dallas TX US 75220 75220
FDA Registration Numbers#
- 3014150341
Source Documents#
Other 510(k) Records For Product Code IXX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K915365 | AP-6CR CINERADIOGRAPHIC FILM PROCESSOR | The Allen Products Co. | 1992-08-27 |
| K913241 | JAMIESON JT-CRP CINE FILM PROCESSOR | Jamieson Film Co. | 1991-09-24 |
| K861928 | STERILE O. R. TOWEL | Anago, Inc. | 1986-06-09 |
| K850421 | CINE RADIOGRAPHIC FILM PROCESSOR M-45CR | The Allen Products Co. | 1985-03-22 |
| K841431 | RADIOGRAPHIC FILM PROCESSOR M-30CR & | The Allen Products Co. | 1984-07-06 |
Legacy Summary#
summary
FDA Review#
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