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

'RAPID ONE' - PROPOXYPHENE TEST

K Number: K030835 · Decision May 22, 2003
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
21
Applicant Total
30
Review Days
66

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Basic Information

Device Name
'RAPID ONE' - PROPOXYPHENE TEST
K Number
K030835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3700
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Bio Medica Corp.
Date Received
March 17, 2003
Decision Date
May 22, 2003
Product Code
JXN
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
JXN Enzyme Immunoassay, Propoxyphene

Similar 510(k) Clearances

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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
K023869 'RAPIDTEC'-5M-MULTIPLE DIP TEST
K021114 'RAPIDTEC' 5A MULTIPLE DIP TEST
K014101 RAPIDONE-OXY TEST
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