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FDA 510(k)

X-RAY APRON

K-Number: K870563 · 1987-02-19

ApplicantX-Tech, Ltd.
Decision Date1987-02-19
Product CodeEAJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

X-RAY APRON is the device name listed in this FDA 510(k) record. The listed applicant is X-Tech, Ltd.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K870563. The device is classified under product code EAJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RAY APRON?

X-RAY APRON is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is X-Tech, Ltd.. The 510(k) number is K870563.

When did X-RAY APRON receive FDA 510(k) clearance?

X-RAY APRON received FDA 510(k) clearance on 1987-02-19, under 510(k) number K870563.

Who is the listed applicant for X-RAY APRON?

The FDA 510(k) record lists X-Tech, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-RAY APRON?

The FDA product code for X-RAY APRON is EAJ.

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: EAJ)

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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