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

CIPRO (TM) DIAGNOSTIC POWDER

K Number: K872081 · Decision Jun 15, 1987
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
13
Applicant Total
2
Review Days
17

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Basic Information

Device Name
CIPRO (TM) DIAGNOSTIC POWDER
K Number
K872081
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1640
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Miles Pharmaceuticals
Date Received
May 29, 1987
Decision Date
June 15, 1987
Product Code
JTT
Advisory Committee
Microbiology
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
JTT Susceptibility Test Powders, Antimicrobial

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Other Clearances by Miles Pharmaceuticals

K Number Device Name
K820578 MEZLIN DIAGNOSTIC REAGENT