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Whitmore Ent., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933778WHITMORE ANKLE X-RAY EXTENSION (AXE)December 13, 1993
K931037WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)July 30, 1993