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Core Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K924271
CHIBA/FRANSEEN/WESTCOTT/SPINAL STYLE NEEDLES
November 23, 1992
K924270
BREAST LESION LOCALIZATION NEEDLE
September 23, 1992
K914732
CORE MEDICAL BIOPSY NEEDLE
January 7, 1992