FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

G.E. STERILE BREAST BIOPSY/LOCALIZATION TRAY

K Number: K960201 · Decision Feb 21, 1996
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
169
Review Days
36

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Basic Information

Device Name
G.E. STERILE BREAST BIOPSY/LOCALIZATION TRAY
K Number
K960201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GE Medical Systems
Date Received
January 16, 1996
Decision Date
February 21, 1996
Product Code
FRG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRG Wrap, Sterilization

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