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FDA 510(k)

SENSORMEDICS MODEL 922 SPIROMETER

K-Number: K920246 · 1992-04-08

ApplicantSensor Medics Corp.
Decision Date1992-04-08
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSORMEDICS MODEL 922 SPIROMETER 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 1992-04-08 under 510(k) number K920246. 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 SENSORMEDICS MODEL 922 SPIROMETER?

SENSORMEDICS MODEL 922 SPIROMETER is a medical device that received FDA 510(k) clearance on 1992-04-08. The listed applicant is Sensor Medics Corp.. The 510(k) number is K920246.

When did SENSORMEDICS MODEL 922 SPIROMETER receive FDA 510(k) clearance?

SENSORMEDICS MODEL 922 SPIROMETER received FDA 510(k) clearance on 1992-04-08, under 510(k) number K920246.

Who is the listed applicant for SENSORMEDICS MODEL 922 SPIROMETER?

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 SENSORMEDICS MODEL 922 SPIROMETER?

The FDA product code for SENSORMEDICS MODEL 922 SPIROMETER 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.

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