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

DRYSLIDE CARTARRHALIS

K Number: K954783 · Decision Feb 6, 1996
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
243
Applicant Total
121
Review Days
112

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Basic Information

Device Name
DRYSLIDE CARTARRHALIS
K Number
K954783
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Difco Laboratories, Inc.
Date Received
October 17, 1995
Decision Date
February 6, 1996
Product Code
JTO
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JTO), ordered by most recent decision date.

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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)
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
K934894 CULTURESWAB TRANSPORT SYSTEM
Search all 121 clearances from Difco Laboratories, Inc. →