ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER
K-Number: K051002 · 2005-05-17
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Device Summary
Frequently Asked Questions
What is the ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER?
ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER is a medical device that received FDA 510(k) clearance on 2005-05-17. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K051002.
When did ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER receive FDA 510(k) clearance?
ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER received FDA 510(k) clearance on 2005-05-17, under 510(k) number K051002.
Who is the listed applicant for ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER?
The FDA 510(k) record lists Ethicon Endo-Surgery, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER?
The FDA product code for ENDOPATH ENDOCUTTER 60 ENDOSCOPIC LINEAR CUTTER 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, 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: 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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