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FDA 510(k)

TISSUELINK FLOATING BALL MODEL 23-201-1

K-Number: K032132 · 2003-08-20

ApplicantTissuelink Medical, Inc.
Decision Date2003-08-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TISSUELINK FLOATING BALL MODEL 23-201-1 is the device name listed in this FDA 510(k) record. The listed applicant is Tissuelink Medical, Inc.. It received FDA 510(k) clearance on 2003-08-20 under 510(k) number K032132. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUELINK FLOATING BALL MODEL 23-201-1?

TISSUELINK FLOATING BALL MODEL 23-201-1 is a medical device that received FDA 510(k) clearance on 2003-08-20. The listed applicant is Tissuelink Medical, Inc.. The 510(k) number is K032132.

When did TISSUELINK FLOATING BALL MODEL 23-201-1 receive FDA 510(k) clearance?

TISSUELINK FLOATING BALL MODEL 23-201-1 received FDA 510(k) clearance on 2003-08-20, under 510(k) number K032132.

Who is the listed applicant for TISSUELINK FLOATING BALL MODEL 23-201-1?

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

What is the FDA product code for TISSUELINK FLOATING BALL MODEL 23-201-1?

The FDA product code for TISSUELINK FLOATING BALL MODEL 23-201-1 is GEI.

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Other records listing Tissuelink Medical, 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: GEI)

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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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