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FDA 510(k)

AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000

K-Number: K072185 · 2008-03-27

ApplicantAiristar Technologies, LLC
Decision Date2008-03-27
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Airistar Technologies, LLC. It received FDA 510(k) clearance on 2008-03-27 under 510(k) number K072185. 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 AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000?

AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000 is a medical device that received FDA 510(k) clearance on 2008-03-27. The listed applicant is Airistar Technologies, LLC. The 510(k) number is K072185.

When did AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000 receive FDA 510(k) clearance?

AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000 received FDA 510(k) clearance on 2008-03-27, under 510(k) number K072185.

Who is the listed applicant for AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000?

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

What is the FDA product code for AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000?

The FDA product code for AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000 is FRF.

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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.

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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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