OXYMAX— 510(k) K895791

Substantially Equivalent

Columbus Instruments Intl. Corp.

FDA 510(k) clearance K895791 for OXYMAX, Substantially Equivalent on 1990-03-28. Applicant: Columbus Instruments Intl. Corp.. Device class: 2.

Clearance details

Applicant: Columbus Instruments Intl. Corp.
Product code: Code BZL
Device class: Class 2
Regulation: 21 CFR 868.1730
Advisory panel: Anesthesiology
Date received: 1989-09-28
Decision date: 1990-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, OH, US

Download summary PDF View on FDA.gov ↗

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