AT HOME DRUG TEST, MODEL 9175— 510(k) K992217
Substantially EquivalentPhamatech
FDA 510(k) clearance K992217 for AT HOME DRUG TEST, MODEL 9175, Substantially Equivalent on 1999-07-13. Applicant: Phamatech.
Clearance details
- Applicant
- Phamatech
- Product code
- Code MVO
- Advisory panel
- Unknown
- 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.