FDA 510(k)

TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE

K-Number: K851856 · 1985-05-23

Decision Date1985-05-23

Product CodeCBI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Sheridan Catheter Corp.. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K851856. The device is classified under product code CBI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE?

TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K851856.

When did TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE receive FDA 510(k) clearance?

TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851856.

Who is the listed applicant for TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE?

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

What is the FDA product code for TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE?

The FDA product code for TRACHEAL/BRONCHIAL DIFFERENTIAL VENTILATION TUBE is CBI.

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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.