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FDA 510(k)

ATRICURE DISSECTOR

K-Number: K041681 · 2004-07-01

ApplicantAtriCure, Inc.
Decision Date2004-07-01
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATRICURE DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is AtriCure, Inc.. It received FDA 510(k) clearance on 2004-07-01 under 510(k) number K041681. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATRICURE DISSECTOR?

ATRICURE DISSECTOR is a medical device that received FDA 510(k) clearance on 2004-07-01. The listed applicant is AtriCure, Inc.. The 510(k) number is K041681.

When did ATRICURE DISSECTOR receive FDA 510(k) clearance?

ATRICURE DISSECTOR received FDA 510(k) clearance on 2004-07-01, under 510(k) number K041681.

Who is the listed applicant for ATRICURE DISSECTOR?

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

What is the FDA product code for ATRICURE DISSECTOR?

The FDA product code for ATRICURE DISSECTOR is FTD.

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Other records listing AtriCure, Inc. as applicant

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Related Devices (Code: FTD)

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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