ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK
K-Number: K131663 · 2013-10-18
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Device Summary
Frequently Asked Questions
What is the ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK?
ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK is a medical device that received FDA 510(k) clearance on 2013-10-18. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K131663.
When did ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK receive FDA 510(k) clearance?
ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK received FDA 510(k) clearance on 2013-10-18, under 510(k) number K131663.
Who is the listed applicant for ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK?
The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK?
The FDA product code for ECHELON ENDOSCOPIC LINEAR CUTTER RELOAD, BLACK is GDW.
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 Endo-Surgery, LLC 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: GDW)
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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