DOTRICH ELECTRONIC AIR CLEANER #C500AM
K-Number: K812656 · 1981-10-08
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Device Summary
Frequently Asked Questions
What is the DOTRICH ELECTRONIC AIR CLEANER #C500AM?
DOTRICH ELECTRONIC AIR CLEANER #C500AM is a medical device that received FDA 510(k) clearance on 1981-10-08. The listed applicant is Leedal, Inc.. The 510(k) number is K812656.
When did DOTRICH ELECTRONIC AIR CLEANER #C500AM receive FDA 510(k) clearance?
DOTRICH ELECTRONIC AIR CLEANER #C500AM received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812656.
Who is the listed applicant for DOTRICH ELECTRONIC AIR CLEANER #C500AM?
The FDA 510(k) record lists Leedal, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOTRICH ELECTRONIC AIR CLEANER #C500AM?
The FDA product code for DOTRICH ELECTRONIC AIR CLEANER #C500AM 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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