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FDA 510(k)

ADVANTAGE PADDLE

K-Number: K033202 · 2003-12-03

Decision Date2003-12-03
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANTAGE PADDLE is the device name listed in this FDA 510(k) record. The listed applicant is Livingston Products, Inc.. It received FDA 510(k) clearance on 2003-12-03 under 510(k) number K033202. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANTAGE PADDLE?

ADVANTAGE PADDLE is a medical device that received FDA 510(k) clearance on 2003-12-03. The listed applicant is Livingston Products, Inc.. The 510(k) number is K033202.

When did ADVANTAGE PADDLE receive FDA 510(k) clearance?

ADVANTAGE PADDLE received FDA 510(k) clearance on 2003-12-03, under 510(k) number K033202.

Who is the listed applicant for ADVANTAGE PADDLE?

The FDA 510(k) record lists Livingston Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVANTAGE PADDLE?

The FDA product code for ADVANTAGE PADDLE is IZH.

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.

Related Devices (Code: IZH)

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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