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FDA 510(k), K943998, CANNABINOID EIA ASSAY
FDA 510(k), K943998, CANNABINOID EIA ASSAY
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510(K) Number: K943998
Device Name: CANNABINOID EIA ASSAY
Manufacturer: DIAGNOSTIC REAGENTS, INC.
Device Classification Name: enzyme immunoassay, cannabinoids
Regulation Number: 862.3870
Classification Product Code: LDJ
Date Received: 06/21/1994
Decision Date: 11/04/1994
Regulation Medical Specialty: Toxicology
Device Name: CANNABINOID EIA ASSAY
Manufacturer: DIAGNOSTIC REAGENTS, INC.
Device Classification Name: enzyme immunoassay, cannabinoids
Regulation Number: 862.3870
Classification Product Code: LDJ
Date Received: 06/21/1994
Decision Date: 11/04/1994
Regulation Medical Specialty: Toxicology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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