Reagents, Test, Tetrahydrocannabinol
FDA product code DKE · 12 cleared devices
Class 2
Clinical Toxicology
- Regulation
- 21 CFR 862.3870
- Review panel
- TX
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1980-02-29 – 2000-12-22
DKE
2000-12-22
DKE
2000-06-02
INSTANT-VIEW MARIJUANA URINE CASSETTE TEST
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DKE
1999-07-06
STATUS STIK, ACCUSIGN STIK
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DKE
1999-06-18
STATUS CUP ACCUSIGN CUP
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DKE
1999-04-15
ACCUSIGN DOA8, DOA8 PANEL, THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA8, THC/OPI/COC/AMP/BZO/BAR/TCA/PAP, STATUS DS DO8
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DKE
1998-09-28
ACCUSIGN DOA 8, ACCUSIGN DOA 8 PANEL, ACCUSIGN THC/OPI/COC/AMP/BZO/BAR/TCA/PCP, BIOSIGN DOA 8, BIOSIGN THC/OPI/COC/AMP/P
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DKE
1998-07-29
PROFILE-II MODEL 600582
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DKE
1990-06-01
SPEC(TM) EXTRACTION CARTRIDGE
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DKE
1988-07-05
MODIFIED LABELING FOR TOXI-LAB THC SCREEN
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DKE
1984-07-06
CANNU-SKREEN-PRELIMINARY
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DKE
1983-06-30
TOXI-LAB CANNABINOID THC SCREEN
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DKE
1980-02-29
DRUGALYZER DTK-1000 KIT PRESUMPTIVE DRUG
View details →No matching devices.
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