MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175— 510(k) K003858
Substantially EquivalentPhamatech
FDA 510(k) clearance K003858 for MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175, Substantially Equivalent on 2001-02-12. Applicant: Phamatech. Device class: Unclassified.
Clearance details
- Applicant
- Phamatech
- Product code
- Code MVO
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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More clearances from Phamatech
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