REUSABLE LINEAR STAPLER HANDLE
K-Number: K110049 · 2011-02-10
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Device Summary
Frequently Asked Questions
What is the REUSABLE LINEAR STAPLER HANDLE?
REUSABLE LINEAR STAPLER HANDLE is a medical device that received FDA 510(k) clearance on 2011-02-10. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K110049.
When did REUSABLE LINEAR STAPLER HANDLE receive FDA 510(k) clearance?
REUSABLE LINEAR STAPLER HANDLE received FDA 510(k) clearance on 2011-02-10, under 510(k) number K110049.
Who is the listed applicant for REUSABLE LINEAR STAPLER HANDLE?
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 REUSABLE LINEAR STAPLER HANDLE?
The FDA product code for REUSABLE LINEAR STAPLER HANDLE 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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