Company ยท US
Surgipath
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1982. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 4, 1982 | K820027 | MODIFIED EA 50 Surgipath | HZJ |
| Dec 10, 1981 | K812940 | 10% NEUTRAL BUFFERED FORMALIN CONCENT Surgipath | IFP |
| Aug 13, 1981 | K812087 | EA 50 Surgipath | HZJ |
| Aug 13, 1981 | K812086 | EA 65 Surgipath | HZJ |
| Jul 10, 1981 | K811826 | EOSIN Y Surgipath | HYB |
| Jul 10, 1981 | K811825 | ORANGE G-6 Surgipath | HZH |
| Apr 23, 1981 | K810836 | DECALCIFIER II Surgipath | KDX |
| Apr 14, 1981 | K810760 | GILL'S HEMATOXYLIN #3 Surgipath | |
| Apr 14, 1981 | K810759 | GILL'S HEMATOXYLIN #2 Surgipath | HYJ |
| Apr 14, 1981 | K810758 | GILL'S HEMATOXYLIN #1 Surgipath | HYJ |
| Apr 14, 1981 | K810733 | HARRIS HEMATOXYLIN Surgipath | HYK |
| Mar 6, 1981 | K810323 | ACRYTOL, MOUNTING MEDIUM Surgipath | KEP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||