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FDA 510(k)

NEWDEAL K WIRE

K-Number: K022599 · 2002-10-30

ApplicantNew Deal, S.A.
Decision Date2002-10-30
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEWDEAL K WIRE is the device name listed in this FDA 510(k) record. The listed applicant is New Deal, S.A.. It received FDA 510(k) clearance on 2002-10-30 under 510(k) number K022599. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEWDEAL K WIRE?

NEWDEAL K WIRE is a medical device that received FDA 510(k) clearance on 2002-10-30. The listed applicant is New Deal, S.A.. The 510(k) number is K022599.

When did NEWDEAL K WIRE receive FDA 510(k) clearance?

NEWDEAL K WIRE received FDA 510(k) clearance on 2002-10-30, under 510(k) number K022599.

Who is the listed applicant for NEWDEAL K WIRE?

The FDA 510(k) record lists New Deal, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEWDEAL K WIRE?

The FDA product code for NEWDEAL K WIRE is HTY.

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Other records listing New Deal, S.A. 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: HTY)

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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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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