AT HOME DRUG TEST, MODEL 9133— 510(k) K994236

Name: FDA 510(k) clearance K994236
Creator: U.S. Food and Drug Administration
Published: 1999-12-30

Substantially Equivalent

Phamatech

FDA 510(k) clearance K994236 for AT HOME DRUG TEST, MODEL 9133, Substantially Equivalent on 1999-12-30. Applicant: Phamatech. Device class: Unclassified.

Clearance details

Applicant: Phamatech
Product code: Code LCM
Device class: Unclassified
Advisory panel: Unknown
Date received: 1999-12-16
Decision date: 1999-12-30
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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