Company ยท US
Diacor, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 2013. Name variants (Inc, Corp, punctuation) are merged.
10510(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 |
|---|---|---|---|
| Jan 17, 2013 | K121929 | ZEPHYR 'X-SERIES PATIENT TRANSFER SLED Diacor, Inc. | FRZ |
| May 23, 2005 | K050888 | INTEGRA IMMOBILIZATION SYSTEM Diacor, Inc. | IYE |
| Oct 23, 1995 | K954414 | CENTRALITE BACKPOINTER Diacor, Inc. | IWE |
| Sep 22, 1995 | K953046 | PERI-PUSHER Diacor, Inc. | IYE |
| Aug 16, 1995 | K950112 | CENTRALITE(R)-DLL SERIES Diacor, Inc. | IWE |
| Nov 3, 1993 | K934566 | RADASSIST Diacor, Inc. | IYE |
| Jul 26, 1993 | K930246 | MAMMORX Diacor, Inc. | IYE |
| Aug 17, 1989 | K893398 | CENTRALITE BACKPOINTER Diacor, Inc. | IWE |
| Jul 15, 1987 | K872489 | CENTRALITE Diacor, Inc. | IWE |
| Jan 30, 1986 | K860193 | PORTALCAST Diacor, Inc. | IXI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||