BXJClass I
Clip, Nose
21 CFR 868.6225 / Anesthesiology
BXJ is the FDA product code for Clip, Nose, a class I device type, regulated under 21 CFR 868.6225. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- BXJ
- Device name
- Clip, Nose
- Regulation
- 21 CFR 868.6225
- Device class
- Class I
- Review panel
- Anesthesiology
- 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 BXJ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 1 |
| 1981 | 1 |
| 1985 | 1 |
Applicants with the most clearances
Product code BXJ| Applicant | Clearances |
|---|---|
| BD Becton Dickinson Vacutainer Systems Preanalytic | 1 |
| Inspiron Corp. | 1 |
| Medipart Jerry Alexander | 1 |
| Todd Industries, 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.
