DIGITAL MANOMETER (DM 50)— 510(k) K901998

Name: FDA 510(k) clearance K901998
Creator: U.S. Food and Drug Administration
Published: 1990-07-25

Substantially Equivalent

Medical Support Products, Inc.

FDA 510(k) clearance K901998 for DIGITAL MANOMETER (DM 50), Substantially Equivalent on 1990-07-25. Applicant: Medical Support Products, Inc.. Device class: 2.

Clearance details

Applicant: Medical Support Products, Inc.
Product code: Code BXR
Device class: Class 2
Regulation: 21 CFR 868.1780
Advisory panel: Anesthesiology
Date received: 1990-05-02
Decision date: 1990-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lancaster, PA, US

Download summary PDF View on FDA.gov ↗

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