AIRWAY PRESSURE MONITOR— 510(k) K810753

Name: FDA 510(k) clearance K810753
Creator: U.S. Food and Drug Administration
Published: 1981-03-31

Substantially Equivalent

Impact Instrumentation, Inc.

FDA 510(k) clearance K810753 for AIRWAY PRESSURE MONITOR, Substantially Equivalent on 1981-03-31. Applicant: Impact Instrumentation, Inc.. Device class: 2.

Clearance details

Applicant: Impact Instrumentation, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1981-03-20
Decision date: 1981-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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