FDA Product Code
FDA Product Code KEP — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.4010
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K830659 | CLEARIUM, MOUNTING MEDIUM | Surgipath Medical Industries, Inc. | 1983-03-17 | Traditional | PDF ↗ |
| K810323 | ACRYTOL, MOUNTING MEDIUM | Surgipath | 1981-03-06 | Traditional | PDF ↗ |
| K800847 | ENTELLAN | Mcb Manufacturing Chemists, Inc. | 1980-05-08 | Traditional | PDF ↗ |
Product code KEP · Class I · Pathology. Data: openFDA.