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FDA 510(k)

ETHIBOND EXCEL VALVE LOOP SUTURE

K-Number: K003070 · 2000-11-07

ApplicantETHICON, Inc.
Decision Date2000-11-07
Product CodeDXZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ETHIBOND EXCEL VALVE LOOP SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2000-11-07 under 510(k) number K003070. The device is classified under product code DXZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHIBOND EXCEL VALVE LOOP SUTURE?

ETHIBOND EXCEL VALVE LOOP SUTURE is a medical device that received FDA 510(k) clearance on 2000-11-07. The listed applicant is ETHICON, Inc.. The 510(k) number is K003070.

When did ETHIBOND EXCEL VALVE LOOP SUTURE receive FDA 510(k) clearance?

ETHIBOND EXCEL VALVE LOOP SUTURE received FDA 510(k) clearance on 2000-11-07, under 510(k) number K003070.

Who is the listed applicant for ETHIBOND EXCEL VALVE LOOP SUTURE?

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

What is the FDA product code for ETHIBOND EXCEL VALVE LOOP SUTURE?

The FDA product code for ETHIBOND EXCEL VALVE LOOP SUTURE is DXZ.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: DXZ)

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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