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

GIBCO HERPES ID KIT

K Number: K841943 · Decision Mar 13, 1985
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
36
Applicant Total
67
Review Days
306

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Basic Information

Device Name
GIBCO HERPES ID KIT
K Number
K841943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3305
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Gibco Laboratories Life Technologies, Inc.
Date Received
May 11, 1984
Decision Date
March 13, 1985
Product Code
GQL
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
GQL Antisera, Fluorescent, Herpesvirus Hominis 1,2

Similar 510(k) Clearances

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Other Clearances by Gibco Laboratories Life Technologies, Inc.

K Number Device Name
K871855 SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM
K871541 MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226
K870134 MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PRE
K864755 PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM
K864014 LOMBARD DOWELL AGAR BASE
K863821 MUELLER HINTON AGAR W/4%NACL AND OXACILLIN
K863820 DRI-FORM: GBNA LISTERIA MEDIUM NO. M22300
K863289 CDC ANAEROBIC AGAR W/SHEEP BLOOD, KANA-&VANCOMYCIN
K862425 MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM
K861058 SENSITITRE AUTO ID PLATE, AP70
Search all 67 clearances from Gibco Laboratories Life Technologies, Inc. →