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FDA 510(k)

ANALYZER, PULMONARY FUNCTION

K-Number: K780322 · 1978-03-14

ApplicantHospal Medical Corp.
Decision Date1978-03-14
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANALYZER, PULMONARY FUNCTION is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780322. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, PULMONARY FUNCTION?

ANALYZER, PULMONARY FUNCTION is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Hospal Medical Corp.. The 510(k) number is K780322.

When did ANALYZER, PULMONARY FUNCTION receive FDA 510(k) clearance?

ANALYZER, PULMONARY FUNCTION received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780322.

Who is the listed applicant for ANALYZER, PULMONARY FUNCTION?

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

What is the FDA product code for ANALYZER, PULMONARY FUNCTION?

The FDA product code for ANALYZER, PULMONARY FUNCTION is BZC.

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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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