HPM REPLACEMENT ULPA FILTER MODEL UF001— 510(k) K920371

Name: FDA 510(k) clearance K920371
Creator: U.S. Food and Drug Administration
Published: 1992-08-12

Substantially Equivalent

Hpm Ent.

FDA 510(k) clearance K920371 for HPM REPLACEMENT ULPA FILTER MODEL UF001, Substantially Equivalent on 1992-08-12. Applicant: Hpm Ent.. Device class: 2.

Clearance details

Applicant: Hpm Ent.
Product code: Code FYD
Device class: Class 2
Regulation: 21 CFR 878.5070
Advisory panel: General, Plastic Surgery
Date received: 1992-01-28
Decision date: 1992-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Niguel, CA, US

Download summary PDF View on FDA.gov ↗

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