FDA Product Code
FDA Product Code KER — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.3010
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K831922 | EMBEDDING RING | Polymer Technology Corp. | 1983-07-29 | Traditional | PDF ↗ |
| K831900 | MACLEAN-FOGG, DISP. BASE MOLD | Polymer Technology Corp. | 1983-07-28 | Traditional | PDF ↗ |
| K831333 | EMBEDDING RINGS | Surgipath Medical Industries, Inc. | 1983-05-25 | Traditional | PDF ↗ |
| K831335 | DISPOSABLE BASE MOLD | Surgipath Medical Industries, Inc. | 1983-05-16 | Traditional | PDF ↗ |
| K772149 | LANCER BIOPSY HOLDER | Sherwood Medical Industries | 1977-11-22 | Traditional | PDF ↗ |
Product code KER · Class I · Pathology. Data: openFDA.