FDA 510(k)

TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE

K-Number: K014260 · 2002-03-27

Decision Date2002-03-27

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE 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 2002-03-27 under 510(k) number K014260. 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 SOLID CYLINDER MONOPOLAR DEVICE?

TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE is a medical device that received FDA 510(k) clearance on 2002-03-27. The listed applicant is Tissuelink Medical, Inc.. The 510(k) number is K014260.

When did TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE receive FDA 510(k) clearance?

TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE received FDA 510(k) clearance on 2002-03-27, under 510(k) number K014260.

Who is the listed applicant for TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE?

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 SOLID CYLINDER MONOPOLAR DEVICE?

The FDA product code for TISSUELINK SOLID CYLINDER MONOPOLAR DEVICE is GEI.

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Other records listing Tissuelink Medical, Inc. as applicant

K073495TISSUELINK AQUAMANTYS MALLEABLE BIPOLAR SEALER WITH LIGHT K063639AQUAMANTYS SS4.0 BIPOLAR SEALER, MODEL 23-121-1 K052859AQUAMANTYS PUMP GENERATOR SYSTEM K032132TISSUELINK FLOATING BALL MODEL 23-201-1 K030380TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 K022532TISSUELINK BIPOLAR FLOATING BALL DEVICE

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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.