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

ASO-CUBE(TM)

K Number: K901371 · Decision May 15, 1990
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
36
Applicant Total
121
Review Days
53

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Basic Information

Device Name
ASO-CUBE(TM)
K Number
K901371
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3720
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Difco Laboratories, Inc.
Date Received
March 23, 1990
Decision Date
May 15, 1990
Product Code
GTQ
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
GTQ Antistreptolysin - Titer/Streptolysin O Reagent

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Other Clearances by Difco Laboratories, Inc.

K Number Device Name
K971211 DISPENS-O-DISC SPARFLOXACIN
K971120 DISPENS-O-DISC (TM) LEVOFLOXACIN
K963508 DISPENS-O-DISC MEROPENEM
K961148 CEFEPIME DISPANS-O-DISC (CEFEPLIME - 30MCG)
K954783 DRYSLIDE CARTARRHALIS
K954784 DRYSIDE NEISSERIA
K953129 ESP CULTURE SYSTEM - MYCO
K950706 DRYSLIDE COAGULASE
K944275 DISPENS-O-DISC PIPERACILLIN 100 MCG./TAZOBACTAM 10 MCG.
K941016 DISPENS-O-DISC(TM) NITROCEFIN
Search all 121 clearances from Difco Laboratories, Inc. →