BXJ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Clip, Nose
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.6225
- Medical specialty
- Anesthesiology
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 2000: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MEDIPART DISPOS. NOSE CLIP MP-2001 (K853578) | Medipart Jerry Alexander | 1985-10-29 |
| NOSECLIP #6118 (K810339) | Todd Industries, Inc. | 1981-03-17 |
| NOSECLIP FOR RESP. CARE & PULMON. FUNC. (K770015) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1977-03-16 |
| NOSE CLIP (K760461) | Inspiron Corp. | 1976-08-26 |
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Every clearance here is in the API, with alerts when new ones post.