AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P— 510(k) K983631

Name: FDA 510(k) clearance K983631
Creator: U.S. Food and Drug Administration
Published: 1999-07-01

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K983631 for AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P, Substantially Equivalent on 1999-07-01. Applicant: Instrumentation Industries, Inc.. Device class: 2.

Clearance details

Applicant: Instrumentation Industries, Inc.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 1998-10-15
Decision date: 1999-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethel Park, PA, US

Download summary PDF View on FDA.gov ↗

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