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FDA 510(k)

PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER

K-Number: K760766 · 1976-10-08

ApplicantFraser Sweatman, Inc.
Decision Date1976-10-08
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER is the device name listed in this FDA 510(k) record. The listed applicant is Fraser Sweatman, Inc.. It received FDA 510(k) clearance on 1976-10-08 under 510(k) number K760766. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER?

PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER is a medical device that received FDA 510(k) clearance on 1976-10-08. The listed applicant is Fraser Sweatman, Inc.. The 510(k) number is K760766.

When did PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER receive FDA 510(k) clearance?

PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER received FDA 510(k) clearance on 1976-10-08, under 510(k) number K760766.

Who is the listed applicant for PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER?

The FDA 510(k) record lists Fraser Sweatman, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER?

The FDA product code for PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER is BZR.

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Other records listing Fraser Sweatman, Inc. as applicant

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.

K771299EMERGENCY OXYGEN RESUSCITATORK770911MEDISHIELD JORDON LIFTING FRAMEK770910MEDISHIELD CERVICAL COLLARK761140FRASER SWEATMAN'S DOUBLE MASKK760076ABSORBER, ANESTHESIA CIRCLE SYS, CO2

Related Devices (Code: BZR)

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.

K243917F&P Optiflow Air/Oxygen Flow SourceFisher & Paykel Healthcare, Ltd.K241465Midas Flowmeter; eAVSParker Hannifin CorporationK231895Maxtec MaxBlend2+pMaxtec, LLCK230987FlowStar Analog Mixer FlowmeterBaldus Sedation GmbH & Co. KGK222794FlowStar Touch Digital Mixer FlowmeterBaldus Sedation GmbH & Co. KGK221494Quality Mix Blender, OxymixerDehas Medical Systems GmbH

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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