PFM PROFESSIONAL 7000 SPIROMETER— 510(k) K932278

Name: FDA 510(k) clearance K932278
Creator: U.S. Food and Drug Administration
Published: 1993-12-17

Substantially Equivalent

Advanced Medical Systems, Inc.

FDA 510(k) clearance K932278 for PFM PROFESSIONAL 7000 SPIROMETER, Substantially Equivalent on 1993-12-17. Applicant: Advanced Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Medical Systems, Inc.
Product code: Code BTY
Device class: Class 2
Regulation: 21 CFR 868.1890
Advisory panel: Anesthesiology
Date received: 1993-05-12
Decision date: 1993-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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