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FDA 510(k)

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628

K-Number: K952233 · 1995-06-16

Decision Date1995-06-16
Product CodeEAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1995-06-16 under 510(k) number K952233. The device is classified under product code EAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628?

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 is a medical device that received FDA 510(k) clearance on 1995-06-16. The listed applicant is Victoreen, Inc.. The 510(k) number is K952233.

When did CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 receive FDA 510(k) clearance?

CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 received FDA 510(k) clearance on 1995-06-16, under 510(k) number K952233.

Who is the listed applicant for CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628?

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 CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628?

The FDA product code for CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628 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.

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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

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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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