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

MONITECT OXYCODONE DRUG SCREEN CASSETTE TEST, MODEL MC 23, FASTECT OXYCODONE DRUG SCREEN DIPSTICK TEST, MODEL MD23

K Number: K030113 · Decision Jul 2, 2003
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
13
Review Days
170

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Basic Information

Device Name
MONITECT OXYCODONE DRUG SCREEN CASSETTE TEST, MODEL MC 23, FASTECT OXYCODONE DRUG SCREEN DIPSTICK TEST, MODEL MD23
K Number
K030113
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Branan Medical Corp.
Date Received
January 13, 2003
Decision Date
July 2, 2003
Product Code
DJG
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
DJG Enzyme Immunoassay, Opiates

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Other Clearances by Branan Medical Corp.

K Number Device Name
K122633 TOXCUP DRUG SCREEN CUP
K122752 FASTECT II PPX DRUG SCREEN DIPSTICK, FASTECT II DRUG SCREEN DIPSTICK, QUICKTOX DRUG SCREEN DIPCARD
K040203 MONITECT MDMA DRUG SCREEN CASSETTE TEST, MODEL MC22; FASTECT II MDMA DRUG SCREEN DIPSTICK TEST, MODEL MF22
K032057 TOXCUP DRUG SCREEN CUP AMP/COC/MET/OPI/PCP/THC
K023489 QUICKTOX MULTIPLE DRUG DIPCARD
K022355 QUICKTOX MULTIPLE DRUG DIPCARD COC/MET/THC/AMP/PCP/BZO/BAR/MTD/TCA, MODEL QT61
K013124 MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP
K012541 MODIFICATION TO:FASTIX THC/COC DRUG SCREEN DIPSTICK TEST, FASTIX THC/COC/MET DRUG SCREEN DIPSTICK TEST, FASTIX OPI/MET
K010734 BRANAN MEDICAL CORPERATION MONITECT TCA DRUG SCREEN TEST, MODEL MC21 AND MD21
K004034 MONITECT MULTIPLE DRUG SCREEN TESTS, MODEL BC12,BC14,TC10,PC11, AND PC12
Search all 13 clearances from Branan Medical Corp. →