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FDA 510(k)

BRONCHODILATOR TEE - 9056 SERIES

K-Number: K873521 · 1988-03-02

ApplicantBoehringer Laboratories
Decision Date1988-03-02
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BRONCHODILATOR TEE - 9056 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1988-03-02 under 510(k) number K873521. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRONCHODILATOR TEE - 9056 SERIES?

BRONCHODILATOR TEE - 9056 SERIES is a medical device that received FDA 510(k) clearance on 1988-03-02. The listed applicant is Boehringer Laboratories. The 510(k) number is K873521.

When did BRONCHODILATOR TEE - 9056 SERIES receive FDA 510(k) clearance?

BRONCHODILATOR TEE - 9056 SERIES received FDA 510(k) clearance on 1988-03-02, under 510(k) number K873521.

Who is the listed applicant for BRONCHODILATOR TEE - 9056 SERIES?

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

What is the FDA product code for BRONCHODILATOR TEE - 9056 SERIES?

The FDA product code for BRONCHODILATOR TEE - 9056 SERIES is CAF.

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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.

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