Whitmore Ent., Inc.

FDA Regulatory Profile

Whitmore Ent., Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 13, 1993.

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