FDA Product Code
FDA Product Code KFK — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4820
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K893949 | #157 EXAM LIGHT | Medmark, Inc. | 1989-08-07 | Traditional | PDF ↗ |
| K894301 | MICRO-AIRE STERNUM SAW 4800 | Micro Surgical Instruments Corp. | 1989-08-03 | Traditional | PDF ↗ |
| K870157 | OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER | Micro-Aire Surgical Instruments, Inc. | 1987-02-24 | Traditional | PDF ↗ |
| K801737 | STERNUM SAW | Amsco Co. | 1980-08-20 | Traditional | PDF ↗ |
Product code KFK · Class I · General, Plastic Surgery. Data: openFDA.