Company ยท US
Proact, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2006. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Apr 12, 2006 | K052243 | PROACT WITH GEL OR PROACT 1 Proact, Inc. | JOW |
| Jun 13, 2001 | K003909 | PROACT 1 Proact Co. | IRP |
| Jul 13, 1994 | K941256 | QUICK CORE II Proact, Ltd. | KNW |
| Mar 22, 1993 | K926559 | PROACT BIOPSY NEEDLE ENCHANCEMENTS Proact, Ltd. | FCG |
| Nov 1, 1991 | K913306 | BONE-TEMNO/STERNUM-TEMNO Proact, Ltd. | LWE |
| Oct 1, 1990 | K902320 | BAUER FLEXI-TEMNO BIOPSY NEEDLE Proact, Ltd. | FCG |
| Sep 6, 1990 | K902319 | BAUER TEMNO BIOPSY NEEDLE Proact, Ltd. | FCG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||