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Allied Biomedical Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K982051KELOCATE SHEETINGAugust 5, 1998
K971478DURALASTIC ANATOMICAL CHIN IMPLANTSJuly 18, 1997
K971479DURALASTIC ANATOMICAL MALAR IMPLANTSJuly 18, 1997
K971481DURALASTIC ANATOMICAL NASAL IMPLANTSJuly 18, 1997
K971480DURALASTIC I AND DURALASTIC IIMay 28, 1997
K955370DURALASTIC IIFebruary 8, 1996
K955368DURALASTIC IFebruary 8, 1996
K955433DURALASTIC SILICONE TUBINGJanuary 26, 1996
K954413KELOCOTENovember 29, 1995