MODULAR X-RAY BARRIERS
K-Number: K850814 · 1985-04-10
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Device Summary
Frequently Asked Questions
What is the MODULAR X-RAY BARRIERS?
MODULAR 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 K850814.
When did MODULAR X-RAY BARRIERS receive FDA 510(k) clearance?
MODULAR X-RAY BARRIERS received FDA 510(k) clearance on 1985-04-10, under 510(k) number K850814.
Who is the listed applicant for MODULAR 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 MODULAR X-RAY BARRIERS?
The FDA product code for MODULAR X-RAY BARRIERS 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.
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: 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
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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