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FDA 510(k)

BRETHANCER, DRUG DELIVERY SYS-INHAL

K-Number: K833922 · 1983-12-08

ApplicantCiba-Geigy Corp.
Decision Date1983-12-08
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BRETHANCER, DRUG DELIVERY SYS-INHAL is the device name listed in this FDA 510(k) record. The listed applicant is Ciba-Geigy Corp.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K833922. 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 BRETHANCER, DRUG DELIVERY SYS-INHAL?

BRETHANCER, DRUG DELIVERY SYS-INHAL is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Ciba-Geigy Corp.. The 510(k) number is K833922.

When did BRETHANCER, DRUG DELIVERY SYS-INHAL receive FDA 510(k) clearance?

BRETHANCER, DRUG DELIVERY SYS-INHAL received FDA 510(k) clearance on 1983-12-08, under 510(k) number K833922.

Who is the listed applicant for BRETHANCER, DRUG DELIVERY SYS-INHAL?

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

What is the FDA product code for BRETHANCER, DRUG DELIVERY SYS-INHAL?

The FDA product code for BRETHANCER, DRUG DELIVERY SYS-INHAL is CAF.

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Other records listing Ciba-Geigy Corp. as applicant

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Official Source

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