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FDA 510(k)

ROBIN HOOD VEST

K-Number: K051300 · 2005-12-08

ApplicantKamber Corporation
Decision Date2005-12-08
Product CodeFRP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ROBIN HOOD VEST is the device name listed in this FDA 510(k) record. The listed applicant is Kamber Corporation. It received FDA 510(k) clearance on 2005-12-08 under 510(k) number K051300. The device is classified under product code FRP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROBIN HOOD VEST?

ROBIN HOOD VEST is a medical device that received FDA 510(k) clearance on 2005-12-08. The listed applicant is Kamber Corporation. The 510(k) number is K051300.

When did ROBIN HOOD VEST receive FDA 510(k) clearance?

ROBIN HOOD VEST received FDA 510(k) clearance on 2005-12-08, under 510(k) number K051300.

Who is the listed applicant for ROBIN HOOD VEST?

The FDA 510(k) record lists Kamber Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROBIN HOOD VEST?

The FDA product code for ROBIN HOOD VEST is FRP.

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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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