JRRClass I
Regulator, Temperature
21 CFR 862.2050 / Clinical Chemistry
JRR is the FDA product code for Regulator, Temperature, a class I device type, regulated under 21 CFR 862.2050. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- JRR
- Device name
- Regulator, Temperature
- Regulation
- 21 CFR 862.2050
- Device class
- Class I
- Review panel
- Clinical Chemistry
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- Yes
- Third party review eligible
- No
- Ingested clearances
- 4
- Ingested recalls
- 0
Clearances, product code JRR
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1978 | 1 |
| 1980 | 1 |
| 1982 | 1 |
Applicants with the most clearances
Product code JRR| Applicant | Clearances |
|---|---|
| American Dade | 1 |
| Gorman Rupp Industries | 1 |
| Streck Laboratories, Inc. | 1 |
| Therapac, Inc. | 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.
