FDA 510(k)

KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE

K-Number: K961977 · 1996-07-31

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health

Decision Date1996-07-31

Product CodeCBI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1996-07-31 under 510(k) number K961977. 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 KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE?

KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE is a medical device that received FDA 510(k) clearance on 1996-07-31. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K961977.

When did KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE receive FDA 510(k) clearance?

KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE received FDA 510(k) clearance on 1996-07-31, under 510(k) number K961977.

Who is the listed applicant for KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE?

The FDA product code for KENDALL SHER-I-BRONCH ENDOBROCHIAL TUBE is CBI.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health as applicant

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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.