FDA Product Code
FDA Product Code NZD — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General Hospital
- 21 CFR Citation
- 880.6900
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K061721 | PEDI-SPIDER STRAP | Emergency Products and Research | 2006-08-17 | Traditional | PDF ↗ |
Product code NZD · Class I · General Hospital. Data: openFDA.