MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING— 510(k) K853569

Name: FDA 510(k) clearance K853569
Creator: U.S. Food and Drug Administration
Published: 1985-11-07

Substantially Equivalent

Medipart Jerry Alexander

FDA 510(k) clearance K853569 for MEDIPART CORRUGATED POLYETHYLENE & E.V.A. TUBING, Substantially Equivalent on 1985-11-07. Applicant: Medipart Jerry Alexander. Device class: 1.

Clearance details

Applicant: Medipart Jerry Alexander
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1985-08-26
Decision date: 1985-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cary, IL, 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.