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..
Clearance details
- Applicant
- Phamatech, Inc.
- Product code
- Code DJG
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.