MODIFICATION TO AT HOME DRUG TEST, MODELS 9150, 9068, AND 9175— 510(k) K003858

Substantially Equivalent

Phamatech

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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