Diacor, Inc.
Diacor, Inc. appears in FDA public data with 0 recalls, 10 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 17, 2013.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K121929 | ZEPHYR 'X-SERIES PATIENT TRANSFER SLED | January 17, 2013 |
| K050888 | INTEGRA IMMOBILIZATION SYSTEM | May 23, 2005 |
| K954414 | CENTRALITE BACKPOINTER | October 23, 1995 |
| K953046 | PERI-PUSHER | September 22, 1995 |
| K950112 | CENTRALITE(R)-DLL SERIES | August 16, 1995 |
| K934566 | RADASSIST | November 3, 1993 |
| K930246 | MAMMORX | July 26, 1993 |
| K893398 | CENTRALITE BACKPOINTER | August 17, 1989 |
| K872489 | CENTRALITE | July 15, 1987 |
| K860193 | PORTALCAST | January 30, 1986 |