JSDClass I
Culture Media, Selective Broth
21 CFR 866.2360 / Microbiology
JSD is the FDA product code for Culture Media, Selective Broth, a class I device type, regulated under 21 CFR 866.2360. As of , FDA records hold 26 510(k) clearances under this code, the most recent dated , and 2 recalls.
Classification record
- Product code
- JSD
- Device name
- Culture Media, Selective Broth
- Regulation
- 21 CFR 866.2360
- Device class
- Class I
- Review panel
- Microbiology
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 26
- Ingested recalls
- 2
Clearances, product code JSD
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1979 | 4 |
| 1981 | 2 |
| 1982 | 4 |
| 1983 | 4 |
| 1984 | 3 |
| 1985 | 2 |
| 1987 | 5 |
| 1988 | 2 |
Applicants with the most clearances
Product code JSD| Applicant | Clearances |
|---|---|
| Isle Media and Sterile Products, Inc. | 4 |
| Lakewood Biochemical Co., Inc. | 3 |
| BD Becton Dickinson Vacutainer Systems Preanalytic | 2 |
| Granite Diagnostics, Inc. | 2 |
| Micro Media Laboratories | 2 |
| Neogen Culture Media | 1 |
| American Laboratory Supply, Inc. | 1 |
| Apl Medical Supplies | 1 |
| Baxter Healthcare Corporation | 1 |
| Blue Ridge Media Co. | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
