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FDA 510(k)

HEPA 2500 AIR CLEANER

K-Number: K930860 · 1993-12-22

ApplicantTrion, Inc.
Decision Date1993-12-22
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEPA 2500 AIR CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Trion, Inc.. It received FDA 510(k) clearance on 1993-12-22 under 510(k) number K930860. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEPA 2500 AIR CLEANER?

HEPA 2500 AIR CLEANER is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Trion, Inc.. The 510(k) number is K930860.

When did HEPA 2500 AIR CLEANER receive FDA 510(k) clearance?

HEPA 2500 AIR CLEANER received FDA 510(k) clearance on 1993-12-22, under 510(k) number K930860.

Who is the listed applicant for HEPA 2500 AIR CLEANER?

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

What is the FDA product code for HEPA 2500 AIR CLEANER?

The FDA product code for HEPA 2500 AIR CLEANER is FRF.

Related Clinical Trials

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.

Related Devices (Code: FRF)

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.

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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