ECHELON GRAY CARTRIDGE, MODEL ERC45M
K-Number: K080839 · 2008-05-21
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Device Summary
Frequently Asked Questions
What is the ECHELON GRAY CARTRIDGE, MODEL ERC45M?
ECHELON GRAY CARTRIDGE, MODEL ERC45M is a medical device that received FDA 510(k) clearance on 2008-05-21. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K080839.
When did ECHELON GRAY CARTRIDGE, MODEL ERC45M receive FDA 510(k) clearance?
ECHELON GRAY CARTRIDGE, MODEL ERC45M received FDA 510(k) clearance on 2008-05-21, under 510(k) number K080839.
Who is the listed applicant for ECHELON GRAY CARTRIDGE, MODEL ERC45M?
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 GRAY CARTRIDGE, MODEL ERC45M?
The FDA product code for ECHELON GRAY CARTRIDGE, MODEL ERC45M 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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