PENLON BREATHING SYSTEM PRESSURE MONITOR— 510(k) K902381

Name: FDA 510(k) clearance K902381
Creator: U.S. Food and Drug Administration
Published: 1990-08-17

Substantially Equivalent

Penlon, Inc.

FDA 510(k) clearance K902381 for PENLON BREATHING SYSTEM PRESSURE MONITOR, Substantially Equivalent on 1990-08-17. Applicant: Penlon, Inc.. Device class: 2.

Clearance details

Applicant: Penlon, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1990-05-30
Decision date: 1990-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newtown, 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.