FDA Product Code
FDA Product Code MKY — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4320
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K002315 | WISEBANDS SKIN CLOSURE DEVICE | Wisebands , Ltd. | 2001-03-15 | Traditional | PDF ↗ |
| K982439 | PROXIDERM, MODELS TN 460, TN 90 460, BK 460 | Progressive Surgical Products, Inc. | 1998-09-08 | Traditional | PDF ↗ |
| K970439 | PROXIDERM (D-460,D 90 460,D 180,460, PS 460) | Progressive Surgical Products, Inc. | 1997-04-16 | Traditional | PDF ↗ |
| K962144 | PHOENIX ETE TISSUE EXTENSION SYSTEM | Phoenix Biomedical Corp. | 1997-01-14 | Traditional | PDF ↗ |
| K942425 | PROXIDERM (TENTATIVE) | Progressive Surgical Products, Inc. | 1994-11-04 | Traditional | PDF ↗ |
| K942526 | SURE-CLOSURE II 75MM SKIN STRETCHING SYSTEM | Life Medical Sciences, Inc. | 1994-07-19 | Traditional | PDF ↗ |
Product code MKY · Class I · General, Plastic Surgery. Data: openFDA.