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FDA 510(k)

MICRONAIRE ISO-HOOD MAX 5UV

K-Number: K912142 · 1991-10-30

ApplicantMicronaire Corp.
Decision Date1991-10-30
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRONAIRE ISO-HOOD MAX 5UV is the device name listed in this FDA 510(k) record. The listed applicant is Micronaire Corp.. It received FDA 510(k) clearance on 1991-10-30 under 510(k) number K912142. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRONAIRE ISO-HOOD MAX 5UV?

MICRONAIRE ISO-HOOD MAX 5UV is a medical device that received FDA 510(k) clearance on 1991-10-30. The listed applicant is Micronaire Corp.. The 510(k) number is K912142.

When did MICRONAIRE ISO-HOOD MAX 5UV receive FDA 510(k) clearance?

MICRONAIRE ISO-HOOD MAX 5UV received FDA 510(k) clearance on 1991-10-30, under 510(k) number K912142.

Who is the listed applicant for MICRONAIRE ISO-HOOD MAX 5UV?

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

What is the FDA product code for MICRONAIRE ISO-HOOD MAX 5UV?

The FDA product code for MICRONAIRE ISO-HOOD MAX 5UV is EAZ.

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Related Devices (Code: EAZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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