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FDA 510(k)

AIR CARE AIR SANITIZER

K-Number: K860132 · 1987-01-13

ApplicantCooper-Hewitt Electric Co.
Decision Date1987-01-13
Product CodeFRA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AIR CARE AIR SANITIZER is the device name listed in this FDA 510(k) record. The listed applicant is Cooper-Hewitt Electric Co.. It received FDA 510(k) clearance on 1987-01-13 under 510(k) number K860132. 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 AIR CARE AIR SANITIZER?

AIR CARE AIR SANITIZER is a medical device that received FDA 510(k) clearance on 1987-01-13. The listed applicant is Cooper-Hewitt Electric Co.. The 510(k) number is K860132.

When did AIR CARE AIR SANITIZER receive FDA 510(k) clearance?

AIR CARE AIR SANITIZER received FDA 510(k) clearance on 1987-01-13, under 510(k) number K860132.

Who is the listed applicant for AIR CARE AIR SANITIZER?

The FDA 510(k) record lists Cooper-Hewitt Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR CARE AIR SANITIZER?

The FDA product code for AIR CARE AIR SANITIZER is FRA.

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Other records listing Cooper-Hewitt Electric Co. as applicant

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.

K862608SPERTILITE PHOTOTHERAPY LAMPK813050AQUANOMICS, #MP4SFK813045AQUANOMICS, #SP36SFK813047AQUANOMICS, MINI 60LK813046AQUANOMICS, #HHU60K813048AQUANOMICS, #MP2SF

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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.

K252128Zener® (model ZEN-001-B1)Uvx, Inc.K241140ViroZap Indoor Air Purifier, In Duct Model 1008Applied Photonix, LLCK232642AirKEE T900Healkee Medical Pte, Ltd.K232933AirKEE P900Healkee Medical Pte, Ltd.K232645Airgle Room Air PurifierAirgle CorporationK221540Synexis Sphere RxSynexis, LLC

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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