PNEUMOGARD MODEL 1230— 510(k) K781714

Name: FDA 510(k) clearance K781714
Creator: U.S. Food and Drug Administration
Published: 1978-11-27

Substantially Equivalent

Novametrix Medical Systems, Inc.

FDA 510(k) clearance K781714 for PNEUMOGARD MODEL 1230, Substantially Equivalent on 1978-11-27. Applicant: Novametrix Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Novametrix Medical Systems, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1978-10-06
Decision date: 1978-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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