LUPO-TEC— 510(k) K782129

Substantially Equivalent

Armkel, LLC

FDA 510(k) clearance K782129 for LUPO-TEC, Substantially Equivalent on 1979-03-12. Applicant: Armkel, LLC. Device class: 2.

Clearance details

Applicant: Armkel, LLC
Product code: Code DHC
Device class: Class 2
Regulation: 21 CFR 866.5820
Advisory panel: Immunology
Date received: 1978-12-27
Decision date: 1979-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.