FDA Product Code
FDA Product Code PEQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General Hospital
- 21 CFR Citation
- 880.6320
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K131338 | DERMA HOOD | Globalmedia Group, LLC | 2013-07-10 | Traditional | PDF ↗ |
Product code PEQ · Class I · General Hospital. Data: openFDA.