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

CENTRY 2 SYSTEM #016, 103, 016, 104

K Number: K791086 · Decision Jul 3, 1979
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
113
Applicant Total
77
Review Days
21

Basic Information

Device Name
CENTRY 2 SYSTEM #016, 103, 016, 104
K Number
K791086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
COBE LABORATORIES, INC.
Date Received
June 12, 1979
Decision Date
July 3, 1979
Product Code
FIP
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
FIP Subsystem, Water Purification

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