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FDA 510(k)

DOTRICH ELECTRONIC AIR CLEANER #C500AM

K-Number: K812656 · 1981-10-08

ApplicantLeedal, Inc.
Decision Date1981-10-08
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DOTRICH ELECTRONIC AIR CLEANER #C500AM is the device name listed in this FDA 510(k) record. The listed applicant is Leedal, Inc.. It received FDA 510(k) clearance on 1981-10-08 under 510(k) number K812656. 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 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

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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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