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

BC BRUSHES

K Number: K902737 · Decision Aug 24, 1990
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
43
Applicant Total
142
Review Days
64

Basic Information

Device Name
BC BRUSHES
K Number
K902737
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
June 21, 1990
Decision Date
August 24, 1990
Product Code
FDX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FDX Endoscopic Cytology Brush

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