PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS— 510(k) K863033

Name: FDA 510(k) clearance K863033
Creator: U.S. Food and Drug Administration
Published: 1986-08-20

Substantially Equivalent

Intertech/Ohio

FDA 510(k) clearance K863033 for PATIENT GAS SAMPLING KIT/5STAND ALONE VERSIONS, Substantially Equivalent on 1986-08-20. Applicant: Intertech/Ohio. Device class: 1.

Clearance details

Applicant: Intertech/Ohio
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1986-08-11
Decision date: 1986-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Myers, FL, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.