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

RAPID DRUG SCREEN

K Number: K964900 · Decision Apr 14, 1997
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
144
Applicant Total
30
Review Days
138

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Basic Information

Device Name
RAPID DRUG SCREEN
K Number
K964900
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3250
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
American Bio Medica Corp.
Date Received
November 27, 1996
Decision Date
April 14, 1997
Product Code
DIO
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
DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Similar 510(k) Clearances

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

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Other Clearances by American Bio Medica Corp.

K Number Device Name
K170222 Rapid Tox Cup II
K073078 RAPID TOX CUP
K060760 RAPIDONE-BUPRENORPHINE TEST
K053422 RAPIDONE-COCAINE-150 TEST
K053359 RAPIDTOX
K041696 RAPID READER
K041712 'RAPIDTEC 4' TEST
K030835 'RAPID ONE' - PROPOXYPHENE TEST
K023869 'RAPIDTEC'-5M-MULTIPLE DIP TEST
K021114 'RAPIDTEC' 5A MULTIPLE DIP TEST
Search all 30 clearances from American Bio Medica Corp. →