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FDA 510(k)

DERMABOND NX ADHESIVE MODEL: DNX6, DNX12

K-Number: K100423 · 2010-05-04

ApplicantETHICON, Inc.
Decision Date2010-05-04
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DERMABOND NX ADHESIVE MODEL: DNX6, DNX12 is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 2010-05-04 under 510(k) number K100423. The device is classified under product code MPN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMABOND NX ADHESIVE MODEL: DNX6, DNX12?

DERMABOND NX ADHESIVE MODEL: DNX6, DNX12 is a medical device that received FDA 510(k) clearance on 2010-05-04. The listed applicant is ETHICON, Inc.. The 510(k) number is K100423.

When did DERMABOND NX ADHESIVE MODEL: DNX6, DNX12 receive FDA 510(k) clearance?

DERMABOND NX ADHESIVE MODEL: DNX6, DNX12 received FDA 510(k) clearance on 2010-05-04, under 510(k) number K100423.

Who is the listed applicant for DERMABOND NX ADHESIVE MODEL: DNX6, DNX12?

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 DERMABOND NX ADHESIVE MODEL: DNX6, DNX12?

The FDA product code for DERMABOND NX ADHESIVE MODEL: DNX6, DNX12 is MPN.

Related Clinical Trials

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.

Other records listing ETHICON, 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.

View all 195 devices →

Related Devices (Code: MPN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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