LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier
K-Number: K181488 · 2018-10-30
Device Summary
Frequently Asked Questions
What is the LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier?
LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier is a medical device that received FDA 510(k) clearance on 2018-10-30. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K181488.
When did LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier receive FDA 510(k) clearance?
LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier received FDA 510(k) clearance on 2018-10-30, under 510(k) number K181488.
Who is the listed applicant for LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier?
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 LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier?
The FDA product code for LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier is FZP.
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: FZP)
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.