Ligaclip Titanium Ligating Clip

FDA 510(k) K830503 · ETHICON, Inc.

Substantially Equivalent

510(k) numberK830503

Submission

Device name
Ligaclip Titanium Ligating Clip
Applicant
ETHICON, Inc.
Walker, MI, US
Received
February 16, 1983
Decision date
March 8, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FZP – Clip, Implantable
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4300
Specialty
General, Plastic Surgery
Implant
Yes

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K242541Gem ZipclipFZP · Traditional Synovis Micro Companies Alliance A Subsidiary of…01/15/2025SE
K221495SOLID CLIP™ Single Use Clip ApplierFZP · Traditional Medscope Biotech Co., Ltd.07/18/2024SE
K232970Hem-o-lok® Ligating ClipsFZP · Traditional Teleflex Medical01/12/2024SE
K230966angiOCCLUDE Ligating ClipsFZP · Traditional A2 Medical Systems, LLC09/19/2023SE
K232313LIGACLIP Endoscopic Rotating Multiple Clip Applier 12mm L (ER420); LIGACLIP Endoscopic…FZP · Special Ethicon Endo Surgery, LLC08/29/2023SE

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Questions and answers

When was Ligaclip Titanium Ligating Clip cleared by the FDA?

Ligaclip Titanium Ligating Clip (K830503) received a 510(k) decision of Substantially Equivalent on March 8, 1983, 20 days after the submission was received.

What is the product code of K830503?

The FDA product code is FZP – Clip, Implantable, a Class II (moderate risk) device regulated under 21 CFR 878.4300.