AQUA+TFILTERHME/THME/AQUA+TFILTERHCH/THCH— 510(k) K933597

Name: FDA 510(k) clearance K933597
Creator: U.S. Food and Drug Administration
Published: 1993-11-01

Substantially Equivalent

Arthro-Medic, Inc.

FDA 510(k) clearance K933597 for AQUA+TFILTERHME/THME/AQUA+TFILTERHCH/THCH, Substantially Equivalent on 1993-11-01. Applicant: Arthro-Medic, Inc.. Device class: 1.

Clearance details

Applicant: Arthro-Medic, Inc.
Product code: Code BYD
Device class: Class 1
Regulation: 21 CFR 868.5375
Advisory panel: Anesthesiology
Date received: 1993-07-26
Decision date: 1993-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sweden, SE

Download summary PDF View on FDA.gov ↗

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