510(k) K991824

AT HOME DRUG TEST, MODEL 9171 by Phamatech — Product Code MVO

K991824 is an FDA 510(k) premarket notification submitted by Phamatech for the device "AT HOME DRUG TEST, MODEL 9171". The FDA issued a decision of Substantially Equivalent on June 11, 1999. The device falls under product code MVO (Kit, Test, Multiple, Drugs Of Abuse, Over The Counter), a Class U device. Phamatech has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 11, 1999
Date Received
May 27, 1999
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Test, Multiple, Drugs Of Abuse, Over The Counter
Device Class
Class U
Regulation Number
Review Panel
TX
Submission Type