510(k) K921141

CANNABINOID URINE CONTROLS by Diagnostic Reagents, Inc. — Product Code LAS

K921141 is an FDA 510(k) premarket notification submitted by Diagnostic Reagents, Inc. for the device "CANNABINOID URINE CONTROLS". The FDA issued a decision of Substantially Equivalent on April 17, 1992. The device falls under product code LAS (Drug Specific Control Materials), a Class I device regulated under 21 CFR 862.3280. Diagnostic Reagents, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 17, 1992
Date Received
March 10, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drug Specific Control Materials
Device Class
Class I
Regulation Number
862.3280
Review Panel
TX
Submission Type