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FDA 510(k)

ESOPHAGEAL OBTURATION AIRWAY

K-Number: K761195 · 1976-12-09

ApplicantMckesson Corp.
Decision Date1976-12-09
Product CodeCAO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ESOPHAGEAL OBTURATION AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Mckesson Corp.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761195. The device is classified under product code CAO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESOPHAGEAL OBTURATION AIRWAY?

ESOPHAGEAL OBTURATION AIRWAY is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Mckesson Corp.. The 510(k) number is K761195.

When did ESOPHAGEAL OBTURATION AIRWAY receive FDA 510(k) clearance?

ESOPHAGEAL OBTURATION AIRWAY received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761195.

Who is the listed applicant for ESOPHAGEAL OBTURATION AIRWAY?

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 ESOPHAGEAL OBTURATION AIRWAY?

The FDA product code for ESOPHAGEAL OBTURATION AIRWAY is CAO.

Related Clinical Trials

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.

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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 MASKK761194HLR QUICK-FIT HEART-LUNG RESUSCITATORK760017CONSIOUS SEDATION (ANALOR P-76)

Related Devices (Code: CAO)

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.

K971348FASTTRACH SINGLE-PASS TRACHEAL/ESOPHAGEAL AIRWAY SYSTEMGreen Field Medical Sourcing, Inc.K894032EVAC-TUBESharn, Inc.K875226ESOPHAGEAL OBTURATOR/TRACHEAL TUBESheridan Catheter Corp.K864200VETA/VENTED ESOPHAGEAL TUBE AIRWAYCranco Co.K863172RESPIRONICS PTL REVIVEEASYRespironics, Inc.

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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