JNOClass I
N-Benzoyl-L-Arginine Ethyl Ester (U.V.), Trypsin
21 CFR 862.1725 / Clinical Chemistry
JNO is the FDA product code for N-Benzoyl-L-Arginine Ethyl Ester (U.V.), Trypsin, a class I device type, regulated under 21 CFR 862.1725. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and 2 recalls.
Classification record
- Product code
- JNO
- Device name
- N-Benzoyl-L-Arginine Ethyl Ester (U.V.), Trypsin
- Regulation
- 21 CFR 862.1725
- Device class
- Class I
- Review panel
- Clinical Chemistry
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 7
- Ingested recalls
- 2
Clearances, product code JNO
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1981 | 1 |
| 1986 | 1 |
| 1989 | 1 |
| 1993 | 1 |
| 2010 | 1 |
| 2011 | 1 |
Applicants with the most clearances
Product code JNO| Applicant | Clearances |
|---|---|
| BD Becton Dickinson Vacutainer Systems Preanalytic | 1 |
| Cis Radiopharmaceuticals, Inc. | 1 |
| Microanalytic Research, Inc. | 1 |
| Microbiological Research Corp. | 1 |
| Nuclear Diagnostics, Inc. | 1 |
| Wallac Oy, A Subsidiary of Perkinelmer, Inc. | 1 |
| Wallac Oy, Subsidiary of Perkinelmer | 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.
