OXY-ON DIGITAL OXYGEN TIMER— 510(k) K781039

Name: FDA 510(k) clearance K781039
Creator: U.S. Food and Drug Administration
Published: 1978-08-31

Substantially Equivalent

Chambers & Sadler Mfg.

FDA 510(k) clearance K781039 for OXY-ON DIGITAL OXYGEN TIMER, Substantially Equivalent on 1978-08-31. Applicant: Chambers & Sadler Mfg.. Device class: 1.

Clearance details

Applicant: Chambers & Sadler Mfg.
Product code: Code BXP
Device class: Class 1
Regulation: 21 CFR 868.2885
Advisory panel: Anesthesiology
Date received: 1978-06-19
Decision date: 1978-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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