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FDA 510(k)

VETA/VENTED ESOPHAGEAL TUBE AIRWAY

K-Number: K864200 · 1987-03-17

ApplicantCranco Co.
Decision Date1987-03-17
Product CodeCAO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VETA/VENTED ESOPHAGEAL TUBE AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Cranco Co.. It received FDA 510(k) clearance on 1987-03-17 under 510(k) number K864200. 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 VETA/VENTED ESOPHAGEAL TUBE AIRWAY?

VETA/VENTED ESOPHAGEAL TUBE AIRWAY is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is Cranco Co.. The 510(k) number is K864200.

When did VETA/VENTED ESOPHAGEAL TUBE AIRWAY receive FDA 510(k) clearance?

VETA/VENTED ESOPHAGEAL TUBE AIRWAY received FDA 510(k) clearance on 1987-03-17, under 510(k) number K864200.

Who is the listed applicant for VETA/VENTED ESOPHAGEAL TUBE AIRWAY?

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

What is the FDA product code for VETA/VENTED ESOPHAGEAL TUBE AIRWAY?

The FDA product code for VETA/VENTED ESOPHAGEAL TUBE AIRWAY is CAO.

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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.K863172RESPIRONICS PTL REVIVEEASYRespironics, Inc.K761195ESOPHAGEAL OBTURATION AIRWAYMckesson Corp.

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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