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

CAMSYS 6300

K Number: K920574 · Decision Feb 17, 1993
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
6
Applicant Total
12
Review Days
376

Basic Information

Device Name
CAMSYS 6300
K Number
K920574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1620
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
F.M. WIEST USA, INC.
Date Received
February 7, 1992
Decision Date
February 17, 1993
Product Code
EXQ
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
EXQ Cystometer, Electrical Recording

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