JSGClass I
Culture Media, Non-Selective And Non-Differential
21 CFR 866.2300 / Microbiology
JSG is the FDA product code for Culture Media, Non-Selective And Non-Differential, a class I device type, regulated under 21 CFR 866.2300. As of , FDA records hold 209 510(k) clearances under this code, the most recent dated , and 29 recalls.
Classification record
- Product code
- JSG
- Device name
- Culture Media, Non-Selective And Non-Differential
- Regulation
- 21 CFR 866.2300
- 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
- 209
- Ingested recalls
- 29
Clearances, product code JSG
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1976 | 2 |
| 1978 | 1 |
| 1979 | 22 |
| 1980 | 11 |
| 1981 | 30 |
| 1982 | 6 |
| 1983 | 17 |
| 1984 | 25 |
| 1985 | 20 |
| 1986 | 9 |
| 1987 | 38 |
| 1988 | 28 |
Applicants with the most clearances
Product code JSG| Applicant | Clearances |
|---|---|
| Neogen Culture Media | 42 |
| Lakewood Biochemical Co., Inc. | 28 |
| Otisville Biotech, Inc. | 17 |
| Isle Media and Sterile Products, Inc. | 15 |
| Hardy Media | 13 |
| bioMerieux, Inc. | 13 |
| Micro Media Laboratories | 10 |
| Anaerobe Systems | 8 |
| American Laboratory Supply, Inc. | 7 |
| BD Becton Dickinson Vacutainer Systems Preanalytic | 5 |
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.
