KCN
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Ear Wick
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.5220
- Medical specialty
- Ear, Nose, Throat
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| NASOPORE EAR, MODELS ND04, ND05 (K062540) | Polyganics B.V., | 2006-10-18 |
| INVOTEC EAR TAMPON (WICK) W/STRING (K973578) | Invotec International, Inc. | 1997-11-06 |
| ULTRACELL EAR WICK (K920357) | Ultracell Medical Technologies, Inc. | 1993-02-01 |
| POPE OTO-WICK, STERILE & NON-STERILE (K791059) | Xomed, Inc. | 1979-07-17 |
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Every clearance here is in the API, with alerts when new ones post.