DIGITAL CUFF PV GAUGE— 510(k) K900755

Name: FDA 510(k) clearance K900755
Creator: U.S. Food and Drug Administration
Published: 1990-04-26

Substantially Equivalent

International Medical Products, Inc.

FDA 510(k) clearance K900755 for DIGITAL CUFF PV GAUGE, Substantially Equivalent on 1990-04-26. Applicant: International Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: International Medical Products, Inc.
Product code: Code BSK
Device class: Class 2
Regulation: 21 CFR 868.5750
Advisory panel: Anesthesiology
Date received: 1990-02-16
Decision date: 1990-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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