510(k) K013409
K013409 is an FDA 510(k) premarket notification submitted by Phamatech, Inc. for the device "AT HOME DRUG TEST, MODEL 9074". The FDA issued a decision of Substantially Equivalent on December 6, 2001. The device falls under product code MVO (Kit, Test, Multiple, Drugs Of Abuse, Over The Counter), a Class U device. Phamatech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 6, 2001
- Date Received
- October 15, 2001
- 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