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FDA 510(k)

SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS

K-Number: K923988 · 1993-10-21

ApplicantSensor Medics Corp.
Decision Date1993-10-21
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS 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 1993-10-21 under 510(k) number K923988. 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 2200 PULMONARY FUNCTION LABS?

SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS is a medical device that received FDA 510(k) clearance on 1993-10-21. The listed applicant is Sensor Medics Corp.. The 510(k) number is K923988.

When did SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS receive FDA 510(k) clearance?

SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS received FDA 510(k) clearance on 1993-10-21, under 510(k) number K923988.

Who is the listed applicant for SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS?

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 2200 PULMONARY FUNCTION LABS?

The FDA product code for SENSORMEDICS MODEL 2200 PULMONARY FUNCTION LABS 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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