The following data is part of a premarket notification filed by Phamatech with the FDA for At Home Drug Test, Model 9063.
Device ID | K994237 |
510k Number | K994237 |
Device Name: | AT HOME DRUG TEST, MODEL 9063 |
Classification | Enzyme Immunoassay, Amphetamine |
Applicant | PHAMATECH 9265 ACTIVITY RD., #112-113 San Diego, CA 92126 |
Contact | Carl A Mongiovi |
Correspondent | Carl A Mongiovi PHAMATECH 9265 ACTIVITY RD., #112-113 San Diego, CA 92126 |
Product Code | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-12-16 |
Decision Date | 1999-12-30 |
Summary: | summary |