The following data is part of a premarket notification filed by Phamatech with the FDA for At Home Drug Test, Model 9171.
| Device ID | K991824 |
| 510k Number | K991824 |
| Device Name: | AT HOME DRUG TEST, MODEL 9171 |
| Classification | Kit, Test, Multiple, Drugs Of Abuse, Over The Counter |
| 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 | MVO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-05-27 |
| Decision Date | 1999-06-11 |
| Summary: | summary |