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FDA 510(k)

AIR-ELECTRONIC AIR CLEANER (FILTER)

K-Number: K884472 · 1989-01-19

Decision Date1989-01-19
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AIR-ELECTRONIC AIR CLEANER (FILTER) is the device name listed in this FDA 510(k) record. The listed applicant is White-Rodgers, Div. Emerson Electric Co.. It received FDA 510(k) clearance on 1989-01-19 under 510(k) number K884472. 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 AIR-ELECTRONIC AIR CLEANER (FILTER)?

AIR-ELECTRONIC AIR CLEANER (FILTER) is a medical device that received FDA 510(k) clearance on 1989-01-19. The listed applicant is White-Rodgers, Div. Emerson Electric Co.. The 510(k) number is K884472.

When did AIR-ELECTRONIC AIR CLEANER (FILTER) receive FDA 510(k) clearance?

AIR-ELECTRONIC AIR CLEANER (FILTER) received FDA 510(k) clearance on 1989-01-19, under 510(k) number K884472.

Who is the listed applicant for AIR-ELECTRONIC AIR CLEANER (FILTER)?

The FDA 510(k) record lists White-Rodgers, Div. Emerson Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIR-ELECTRONIC AIR CLEANER (FILTER)?

The FDA product code for AIR-ELECTRONIC AIR CLEANER (FILTER) 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

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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