OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING— 510(k) K890011

Name: FDA 510(k) clearance K890011
Creator: U.S. Food and Drug Administration
Published: 1989-03-20

Substantially Equivalent

Life Design Systems, Inc.

FDA 510(k) clearance K890011 for OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING, Substantially Equivalent on 1989-03-20. Applicant: Life Design Systems, Inc.. Device class: 1.

Clearance details

Applicant: Life Design Systems, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1989-01-03
Decision date: 1989-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin, WI, US

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K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

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