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FDA 510(k)

HIOX80 AEROSOL ADAPTER

K-Number: K032516 · 2004-03-04

ApplicantSensor Medics Corp.
Decision Date2004-03-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HIOX80 AEROSOL ADAPTER 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 2004-03-04 under 510(k) number K032516. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIOX80 AEROSOL ADAPTER?

HIOX80 AEROSOL ADAPTER is a medical device that received FDA 510(k) clearance on 2004-03-04. The listed applicant is Sensor Medics Corp.. The 510(k) number is K032516.

When did HIOX80 AEROSOL ADAPTER receive FDA 510(k) clearance?

HIOX80 AEROSOL ADAPTER received FDA 510(k) clearance on 2004-03-04, under 510(k) number K032516.

Who is the listed applicant for HIOX80 AEROSOL ADAPTER?

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 HIOX80 AEROSOL ADAPTER?

The FDA product code for HIOX80 AEROSOL ADAPTER is CAF.

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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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