ENDOPATH
K-Number: K942450 · 1994-08-05
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Device Summary
Frequently Asked Questions
What is the ENDOPATH?
ENDOPATH is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K942450.
When did ENDOPATH receive FDA 510(k) clearance?
ENDOPATH received FDA 510(k) clearance on 1994-08-05, under 510(k) number K942450.
Who is the listed applicant for ENDOPATH?
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?
The FDA product code for ENDOPATH is GBZ.
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: GBZ)
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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