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FDA 510(k)

ALPHA DETECTOR

K-Number: K800319 · 1980-03-03

ApplicantM.O.E Electronics Research & Prod.
Decision Date1980-03-03
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ALPHA DETECTOR is the device name listed in this FDA 510(k) record. The listed applicant is M.O.E Electronics Research & Prod.. It received FDA 510(k) clearance on 1980-03-03 under 510(k) number K800319. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHA DETECTOR?

ALPHA DETECTOR is a medical device that received FDA 510(k) clearance on 1980-03-03. The listed applicant is M.O.E Electronics Research & Prod.. The 510(k) number is K800319.

When did ALPHA DETECTOR receive FDA 510(k) clearance?

ALPHA DETECTOR received FDA 510(k) clearance on 1980-03-03, under 510(k) number K800319.

Who is the listed applicant for ALPHA DETECTOR?

The FDA 510(k) record lists M.O.E Electronics Research & Prod. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALPHA DETECTOR?

The FDA product code for ALPHA DETECTOR is HCC.

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Other records listing M.O.E Electronics Research & Prod. 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.

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Related Devices (Code: HCC)

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.

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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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