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FDA 510(k)

CONSIOUS SEDATION (ANALOR P-76)

K-Number: K760017 · 1976-07-20

ApplicantMckesson Corp.
Decision Date1976-07-20
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONSIOUS SEDATION (ANALOR P-76) is the device name listed in this FDA 510(k) record. The listed applicant is Mckesson Corp.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760017. 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 CONSIOUS SEDATION (ANALOR P-76)?

CONSIOUS SEDATION (ANALOR P-76) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Mckesson Corp.. The 510(k) number is K760017.

When did CONSIOUS SEDATION (ANALOR P-76) receive FDA 510(k) clearance?

CONSIOUS SEDATION (ANALOR P-76) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760017.

Who is the listed applicant for CONSIOUS SEDATION (ANALOR P-76)?

The FDA 510(k) record lists Mckesson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONSIOUS SEDATION (ANALOR P-76)?

The FDA product code for CONSIOUS SEDATION (ANALOR P-76) is BZR.

Related Clinical Trials

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Other records listing Mckesson Corp. 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.

K771175RESUSCITATOR, MS30K761196NITROUS OXIDE SCAVENGING MASKK761195ESOPHAGEAL OBTURATION AIRWAYK761194HLR QUICK-FIT HEART-LUNG RESUSCITATOR

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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