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FDA 510(k)

ED CORP RADIATION SCREEN

K-Number: K944445 · 1995-05-11

ApplicantMed Corp.
Decision Date1995-05-11
Product CodeEAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ED CORP RADIATION SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Med Corp.. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K944445. The device is classified under product code EAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ED CORP RADIATION SCREEN?

ED CORP RADIATION SCREEN is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is Med Corp.. The 510(k) number is K944445.

When did ED CORP RADIATION SCREEN receive FDA 510(k) clearance?

ED CORP RADIATION SCREEN received FDA 510(k) clearance on 1995-05-11, under 510(k) number K944445.

Who is the listed applicant for ED CORP RADIATION SCREEN?

The FDA 510(k) record lists Med Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ED CORP RADIATION SCREEN?

The FDA product code for ED CORP RADIATION SCREEN is EAK.

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: EAK)

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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