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

STC DIAGNOSTICS AUTO-LYTE(TM) ETHYL ALCOHOL ASSAY

K Number: K931516 · Decision Jul 19, 1993
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
32
Applicant Total
28
Review Days
115

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Basic Information

Device Name
STC DIAGNOSTICS AUTO-LYTE(TM) ETHYL ALCOHOL ASSAY
K Number
K931516
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3040
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Solarcare Technologies Corp,Inc.
Date Received
March 26, 1993
Decision Date
July 19, 1993
Product Code
DIC
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
DIC Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method

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Other Clearances by Solarcare Technologies Corp,Inc.

K Number Device Name
K954326 STC DIAGNOSTICS AUTO-LYTE URINARY HEMOGLOBIN ASSAY
K954156 STC DIAGNOSTICS AUTO-LYTE URINARY LEUKOCYTE ESTERASE ASSAY
K955905 STC DIAGNOSTICS AUTO-LYTE URINARY PROTEIN ASSAY
K954158 STC DIAGNOSTICS AUTO-LYTE PH ASSAY
K940048 STC DIAGNOSTICS PCP MICRO-PLATE EIA MODIFICATION
K954073 STC DIAGNOSTICS LSD MICRO-PLATE EIA
K954266 STC DIAGNOSTICS AUTO-LYTE CREATININE ASSAY
K935573 AMPHETAMINES MICRO-PLATE EIA
K935565 OPIATES MICRO-PLATE ASSAY
K950308 STC DIAGNOSTICS AUTO-LYTE(R) METHAQUALONE EIA
Search all 28 clearances from Solarcare Technologies Corp,Inc. →