X-RAY APRON
K-Number: K870563 · 1987-02-19
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Device Summary
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
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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