510(k) K992217

AT HOME DRUG TEST, MODEL 9175 by Phamatech — Product Code MVO

K992217 is an FDA 510(k) premarket notification submitted by Phamatech for the device "AT HOME DRUG TEST, MODEL 9175". The FDA issued a decision of Substantially Equivalent on July 13, 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
July 13, 1999
Date Received
July 1, 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