QUICKSCREEN, MODELS 9177X AND 9178X— 510(k) K041578

Name: FDA 510(k) clearance K041578
Creator: U.S. Food and Drug Administration
Published: 2004-09-10

Substantially Equivalent

Phamatech

FDA 510(k) clearance K041578 for QUICKSCREEN, MODELS 9177X AND 9178X, Substantially Equivalent on 2004-09-10. Applicant: Phamatech. Device class: Unclassified.

Clearance details

Applicant: Phamatech
Product code: Code LCM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2004-06-14
Decision date: 2004-09-10
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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