FDA 510(k)

PULMONARY FUNCTION TESTING STS

K-Number: K840741 · 1984-03-05

Decision Date1984-03-05

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PULMONARY FUNCTION TESTING STS is the device name listed in this FDA 510(k) record. The listed applicant is Circadian, Inc.. It received FDA 510(k) clearance on 1984-03-05 under 510(k) number K840741. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULMONARY FUNCTION TESTING STS?

PULMONARY FUNCTION TESTING STS is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Circadian, Inc.. The 510(k) number is K840741.

When did PULMONARY FUNCTION TESTING STS receive FDA 510(k) clearance?

PULMONARY FUNCTION TESTING STS received FDA 510(k) clearance on 1984-03-05, under 510(k) number K840741.

Who is the listed applicant for PULMONARY FUNCTION TESTING STS?

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

What is the FDA product code for PULMONARY FUNCTION TESTING STS?

The FDA product code for PULMONARY FUNCTION TESTING STS is BZG.

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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.