AIR-ELECTRONIC AIR CLEANER (FILTER)
K-Number: K884472 · 1989-01-19
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Device Summary
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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