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

ACS GENTAMICIN

K Number: K953020 · Decision Aug 2, 1995
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
36
Applicant Total
125
Review Days
34

Basic Information

Device Name
ACS GENTAMICIN
K Number
K953020
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3450
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ciba Corning Diagnostics Corp.
Date Received
June 29, 1995
Decision Date
August 2, 1995
Product Code
LCD
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
LCD Enzyme Immunoassay, Gentamicin

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K Number Device Name
K962559 ACS CORTISOL IMMUNOASSAY
K963251 CIBA CORNING ACS;180 DPD ASSAY
K961807 CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4
K961657 CIBA CORNING 400 SYSTEM
K962021 CIBA CORNING 348 SYSTEM
K962126 ACS CKMB II IMMUNOASSAY
K962041 ACS LH2 IMMUNOASSAY
K961510 ACS FRT4 IMMUNOASSAY
K960246 LIQUID CARDIAC MARKER 1,2,3 ASSAYED
K955873 ACS PHENYTOIN ASSAY
Search all 125 clearances from Ciba Corning Diagnostics Corp. →