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ACCUSIGN DOA 10, ACCUSIGN DOA 10 PANEL, ACUSIGN MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP, BIOSIGN DOA10, BIOSIGN MET/OPI/

FDA 510(k) clearance K990786 · decided 1999-03-26

Clearance details

K-number
K990786
Device name
ACCUSIGN DOA 10, ACCUSIGN DOA 10 PANEL, ACUSIGN MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP, BIOSIGN DOA10, BIOSIGN MET/OPI/
Applicant
Princeton BioMeditech Corp.
Decision
Substantially Equivalent
Date received
1999-03-10
Decision date
1999-03-26
Days to decision
16 days
Clearance type
Special
Product code
LAG
Device class
2
Regulation number
862.3610
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Monmouth Junction, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RAPID TOX CUP (K073078)American Bio Medica Corp.2008-05-30
MODIFICATION TO: ACCUSIGN RC DOA 10 (MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP (K062575)Princeton BioMeditech Corp.2007-11-26
ACCUSIGN DOA 10,ACCUSIGN DOA PANEL,ACCUSIGN MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP,BIOSIGN DOA 10, BIOSIGN MET/OPI/COC/ (K983501)Princeton BioMeditech Corp.1998-12-18

Recalls involving this device

No recalls on record reference this clearance.