MOBILE LEAD PLASTIC X-RAY BARRIERS
K-Number: K850813 · 1985-04-10
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Device Summary
Frequently Asked Questions
What is the MOBILE LEAD PLASTIC X-RAY BARRIERS?
MOBILE LEAD PLASTIC X-RAY BARRIERS is a medical device that received FDA 510(k) clearance on 1985-04-10. The listed applicant is Victoreen, Inc.. The 510(k) number is K850813.
When did MOBILE LEAD PLASTIC X-RAY BARRIERS receive FDA 510(k) clearance?
MOBILE LEAD PLASTIC X-RAY BARRIERS received FDA 510(k) clearance on 1985-04-10, under 510(k) number K850813.
Who is the listed applicant for MOBILE LEAD PLASTIC X-RAY BARRIERS?
The FDA 510(k) record lists Victoreen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOBILE LEAD PLASTIC X-RAY BARRIERS?
The FDA product code for MOBILE LEAD PLASTIC X-RAY BARRIERS is IWX.
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.
Other records listing Victoreen, Inc. 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.
Related Devices (Code: IWX)
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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