Medical Device Manufacturer · US , Salt Lake City , UT

Diacor, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1986

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Diacor, Inc. Radiology ✕

10 devices

1-10 of 10

Cleared Jan 17, 2013

ZEPHYR 'X-SERIES PATIENT TRANSFER SLED

Radiology · 199d

Cleared May 23, 2005

INTEGRA IMMOBILIZATION SYSTEM

Radiology · 46d

Cleared Oct 23, 1995

CENTRALITE BACKPOINTER

Radiology · 32d

Cleared Sep 22, 1995

Radiology · 84d

Cleared Aug 16, 1995

CENTRALITE(R)-DLL SERIES

Radiology · 217d

Cleared Nov 03, 1993

Radiology · 43d

Cleared Jul 26, 1993

Radiology · 188d

Cleared Aug 17, 1989

CENTRALITE BACKPOINTER

Radiology · 108d

Cleared Jul 15, 1987

Radiology · 22d

Cleared Jan 30, 1986

Radiology · 8d