MODIFICATION TO HIOX— 510(k) K030943

Substantially Equivalent

Sensor Medics Corp.

FDA 510(k) clearance K030943 for MODIFICATION TO HIOX, Substantially Equivalent on 2003-04-22. Applicant: Sensor Medics Corp.. Device class: 2.

Clearance details

Applicant: Sensor Medics Corp.
Product code: Code CBP
Device class: Class 2
Regulation: 21 CFR 868.5870
Advisory panel: Anesthesiology
Date received: 2003-03-26
Decision date: 2003-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yorba Linda, CA, 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.