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FDA 510(k)

PULMONARY FUNCTION SYSTEM

K-Number: K842041 · 1984-06-15

ApplicantSensor Medics Corp.
Decision Date1984-06-15
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PULMONARY FUNCTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sensor Medics Corp.. It received FDA 510(k) clearance on 1984-06-15 under 510(k) number K842041. 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 SYSTEM?

PULMONARY FUNCTION SYSTEM is a medical device that received FDA 510(k) clearance on 1984-06-15. The listed applicant is Sensor Medics Corp.. The 510(k) number is K842041.

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

PULMONARY FUNCTION SYSTEM received FDA 510(k) clearance on 1984-06-15, under 510(k) number K842041.

Who is the listed applicant for PULMONARY FUNCTION SYSTEM?

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

What is the FDA product code for PULMONARY FUNCTION SYSTEM?

The FDA product code for PULMONARY FUNCTION SYSTEM is BZG.

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Other records listing Sensor Medics Corp. 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.

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