AT HOME DRUG TEST, MODEL 9079— 510(k) K013408
Substantially EquivalentPhamatech, Inc.
FDA 510(k) clearance K013408 for AT HOME DRUG TEST, MODEL 9079, Substantially Equivalent on 2001-12-06. Applicant: Phamatech, Inc.. Device class: 2.
Clearance details
- Applicant
- Phamatech, Inc.
- Product code
- Code DJG
- Device class
- Class 2
- Regulation
- 21 CFR 862.3650
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- San Diego, CA, US
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