DERMABOND NX ADHESIVE MODEL: DNX6, DNX12
K-Number: K100423 · 2010-05-04
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Device Summary
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.
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
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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