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Delaware Prosthetics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K832151PDM SILOXANE PROSTHETIC ORBITDecember 19, 1983
K832153PDM SILOXANE PROSTHETIC NOSEDecember 9, 1983
K832152PDM SILOXANE PROSTHETIC EARDecember 9, 1983
K832148PDM SILOXANE PROSTHETIC CHIN IMPLANTNovember 28, 1983
K832149PDM SILOXANE PROSTHETIC OBTURATORNovember 28, 1983