AT HOME DRUG TESTT, MODEL 9150 T— 510(k) K010655

Name: FDA 510(k) clearance K010655
Creator: U.S. Food and Drug Administration
Published: 2001-04-05

Substantially Equivalent

Phamatech

FDA 510(k) clearance K010655 for AT HOME DRUG TESTT, MODEL 9150 T, Substantially Equivalent on 2001-04-05. Applicant: Phamatech. Device class: Unclassified.

Clearance details

Applicant: Phamatech
Product code: Code MVO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2001-03-05
Decision date: 2001-04-05
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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K013778 — PEACE OF MIND HOME DRUG TEST2002-02-07
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K010653 — AT HOME DRUG TEST, MODEL 9068 T2001-04-05
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