STERI-VAC(TM) AERATOR MODEL XL— 510(k) K904921

Name: FDA 510(k) clearance K904921
Creator: U.S. Food and Drug Administration
Published: 1990-12-05

Substantially Equivalent

3M Health Care, Ltd.

FDA 510(k) clearance K904921 for STERI-VAC(TM) AERATOR MODEL XL, Substantially Equivalent on 1990-12-05. Applicant: 3M Health Care, Ltd.. Device class: 2.

Clearance details

Applicant: 3M Health Care, Ltd.
Product code: Code FLI
Device class: Class 2
Regulation: 21 CFR 880.6100
Advisory panel: General Hospital
Date received: 1990-10-31
Decision date: 1990-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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