FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.

K Number: K792349 · Decision Mar 12, 1980
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
2
Applicant Total
30
Review Days
114

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Basic Information

Device Name
SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.
K Number
K792349
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1575
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Pfizer, Inc.
Date Received
November 19, 1979
Decision Date
March 12, 1980
Product Code
JNT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JNT Chromatographic, Phospholipids

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