UNIVERSAL OXYGEN TUBING CONNECTOR— 510(k) K840790

Name: FDA 510(k) clearance K840790
Creator: U.S. Food and Drug Administration
Published: 1984-03-30

Substantially Equivalent

Cherry Plastics, Inc.

FDA 510(k) clearance K840790 for UNIVERSAL OXYGEN TUBING CONNECTOR, Substantially Equivalent on 1984-03-30. Applicant: Cherry Plastics, Inc.. Device class: 1.

Clearance details

Applicant: Cherry Plastics, Inc.
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1984-02-03
Decision date: 1984-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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