FDA Product Code
FDA Product Code KIO — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.3800
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K890984 | LINISTAIN SLS | Shandon, Inc. | 1989-04-04 | Traditional | PDF ↗ |
Product code KIO · Class I · Pathology. Data: openFDA.