FDA Product Code
FDA Product Code GFD — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4820
510(k) Clearances — 12 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K965256 | DMS-1000C DERMOABRADER | Mattioli Engineering, Srl | 1996-12-09 | Traditional | PDF ↗ |
| K962371 | DERMTOME BLADE | Dsp Worldwide | 1996-08-29 | Traditional | PDF ↗ |
| K945594 | DECA DERMATOME (MICROMOTOR SYSTEM) | Depuy Intl., Ltd. | 1995-06-05 | Traditional | PDF ↗ |
| K951085 | PADGETT AIR DERMATOME, MODEL A | Padgett Instruments, Inc. | 1995-05-15 | Traditional | PDF ↗ |
| K940208 | AESCULAP ACCU-DERMATOME | Aesculap, Inc. | 1994-02-24 | Traditional | PDF ↗ |
| K862669 | ACTIVATED PARTIAL THROMBOPLASTIN TIME TEST | U. S. Diagnostics, Inc. | 1986-10-03 | Traditional | PDF ↗ |
| K861285 | SKIN MESH DEVICE | Precision Modified Devices | 1986-04-17 | Traditional | PDF ↗ |
| K861138 | MASH DERMATOME | Mecron Medical Products, Inc. | 1986-04-14 | Traditional | PDF ↗ |
| K860925 | DERMASPANDERE | Mri Ventures, Inc. | 1986-03-28 | Traditional | PDF ↗ |
| K842702 | ROSENBERG SKIN GRAFTING KNIVES | Downs Surgical , Ltd. | 1984-08-02 | Traditional | PDF ↗ |
| K830993 | AMPLIGREFFE | Prothia USA, Inc. | 1983-05-03 | Traditional | PDF ↗ |
| K792332 | DAVOL/SIMON DERMATOME | Davol, Inc. | 1979-12-06 | Traditional | PDF ↗ |
Product code GFD · Class I · General, Plastic Surgery. Data: openFDA.