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Diacor, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K121929 ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDFRZ2013-01-17 View
510(k) K050888 INTEGRA IMMOBILIZATION SYSTEMIYE2005-05-23 View
510(k) K954414 CENTRALITE BACKPOINTERIWE1995-10-23 View
510(k) K953046 PERI-PUSHERIYE1995-09-22 View
510(k) K950112 CENTRALITE(R)-DLL SERIESIWE1995-08-16 View
510(k) K934566 RADASSISTIYE1993-11-03 View
510(k) K930246 MAMMORXIYE1993-07-26 View
510(k) K893398 CENTRALITE BACKPOINTERIWE1989-08-17 View
510(k) K872489 CENTRALITEIWE1987-07-15 View
510(k) K860193 PORTALCASTIXI1986-01-30 View
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