AT HOME DRUG TEST MODELS, 9308T AND 9308X— 510(k) K070009
Substantially EquivalentPhamatech, Inc.
FDA 510(k) clearance K070009 for AT HOME DRUG TEST MODELS, 9308T AND 9308X, Substantially Equivalent on 2007-12-07. Applicant: Phamatech, Inc..
Clearance details
- Applicant
- Phamatech, Inc.
- Product code
- Code DIS
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.