AT HOME DRUG CUP, MODEL 9150X— 510(k) K030447

Name: FDA 510(k) clearance K030447
Creator: U.S. Food and Drug Administration
Published: 2003-04-14

Substantially Equivalent

Phamatech

FDA 510(k) clearance K030447 for AT HOME DRUG CUP, MODEL 9150X, Substantially Equivalent on 2003-04-14. Applicant: Phamatech. Device class: Unclassified.

Clearance details

Applicant: Phamatech
Product code: Code MVO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-02-11
Decision date: 2003-04-14
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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