ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS)
K-Number: K972679 · 1997-09-19
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Device Summary
Frequently Asked Questions
What is the ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS)?
ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS) is a medical device that received FDA 510(k) clearance on 1997-09-19. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K972679.
When did ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS) receive FDA 510(k) clearance?
ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS) received FDA 510(k) clearance on 1997-09-19, under 510(k) number K972679.
Who is the listed applicant for ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS)?
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 ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS)?
The FDA product code for ENDOPATH ENDOSCOPIC TISSUE FASTENING SYSTEM (ETFS) is GCJ.
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: GCJ)
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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