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FDA 510(k)

MOBILE LEAD PLASTIC X-RAY BARRIERS

K-Number: K850813 · 1985-04-10

Decision Date1985-04-10
Product CodeIWX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILE LEAD PLASTIC X-RAY BARRIERS is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1985-04-10 under 510(k) number K850813. The device is classified under product code IWX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 40 devices →

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

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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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