UCG-LYPHOTEST— 510(k) K791309

Substantially Equivalent

Wampole Laboratories

FDA 510(k) clearance K791309 for UCG-LYPHOTEST, Substantially Equivalent on 1979-07-30. Applicant: Wampole Laboratories.

Clearance details

Applicant: Wampole Laboratories
Product code: Code JHJ
Advisory panel: Clinical Chemistry
Date received: 1979-07-16
Decision date: 1979-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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