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Diacor, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K121929ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDJanuary 17, 2013
K050888INTEGRA IMMOBILIZATION SYSTEMMay 23, 2005
K954414CENTRALITE BACKPOINTEROctober 23, 1995
K953046PERI-PUSHERSeptember 22, 1995
K950112CENTRALITE(R)-DLL SERIESAugust 16, 1995
K934566RADASSISTNovember 3, 1993
K930246MAMMORXJuly 26, 1993
K893398CENTRALITE BACKPOINTERAugust 17, 1989
K872489CENTRALITEJuly 15, 1987
K860193PORTALCASTJanuary 30, 1986