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FDA 510(k)

TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1

K-Number: K030380 · 2003-03-03

ApplicantTissuelink Medical, Inc.
Decision Date2003-03-03
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 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 2003-03-03 under 510(k) number K030380. 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 SEALING FORCEPS, MODEL 1 21-202-1?

TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Tissuelink Medical, Inc.. The 510(k) number is K030380.

When did TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 receive FDA 510(k) clearance?

TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 received FDA 510(k) clearance on 2003-03-03, under 510(k) number K030380.

Who is the listed applicant for TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1?

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 SEALING FORCEPS, MODEL 1 21-202-1?

The FDA product code for TISSUELINK SEALING FORCEPS, MODEL 1 21-202-1 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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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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