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FDA 510(k)

OXY-ON DIGITAL OXYGEN TIMER

K-Number: K781039 · 1978-08-31

ApplicantChambers & Sadler Mfg.
Decision Date1978-08-31
Product CodeBXP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXY-ON DIGITAL OXYGEN TIMER is the device name listed in this FDA 510(k) record. The listed applicant is Chambers & Sadler Mfg.. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K781039. The device is classified under product code BXP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXY-ON DIGITAL OXYGEN TIMER?

OXY-ON DIGITAL OXYGEN TIMER is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Chambers & Sadler Mfg.. The 510(k) number is K781039.

When did OXY-ON DIGITAL OXYGEN TIMER receive FDA 510(k) clearance?

OXY-ON DIGITAL OXYGEN TIMER received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781039.

Who is the listed applicant for OXY-ON DIGITAL OXYGEN TIMER?

The FDA 510(k) record lists Chambers & Sadler Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXY-ON DIGITAL OXYGEN TIMER?

The FDA product code for OXY-ON DIGITAL OXYGEN TIMER is BXP.

Related Clinical Trials

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Related Devices (Code: BXP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K936141UNIPOWER RECHARGEABLE BATTERY PACKUnipower Corp.K920360TIMOX OXYGEN TIMERMedical Fittings, Inc.K832678PHONATORY FUNCTION ANALYZER PS-77Kells Medical, Inc.K800087ULTRASONIC FLOWMETERThe Perkin-Elmer Corp.K770424OXYGEN TWMER, MODEL SSTTimeter Instrument Corp.K761260ARIZONA OXYGEN TIMER DEVICEThe John Bunn Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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