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FDA 510(k)

UV AIR STERILIGHT

K-Number: K884579 · 1988-12-12

ApplicantAllseasons Environmental Control, Inc.
Decision Date1988-12-12
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UV AIR STERILIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Allseasons Environmental Control, Inc.. It received FDA 510(k) clearance on 1988-12-12 under 510(k) number K884579. The device is classified under product code FRA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UV AIR STERILIGHT?

UV AIR STERILIGHT is a medical device that received FDA 510(k) clearance on 1988-12-12. The listed applicant is Allseasons Environmental Control, Inc.. The 510(k) number is K884579.

When did UV AIR STERILIGHT receive FDA 510(k) clearance?

UV AIR STERILIGHT received FDA 510(k) clearance on 1988-12-12, under 510(k) number K884579.

Who is the listed applicant for UV AIR STERILIGHT?

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

What is the FDA product code for UV AIR STERILIGHT?

The FDA product code for UV AIR STERILIGHT is FRA.

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Related Devices (Code: FRA)

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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