Hemoclip Ligating Clips M/Large

FDA 510(k) K841548 · Edward Weck, Inc.

Substantially Equivalent

510(k) numberK841548

Submission

Device name
Hemoclip Ligating Clips M/Large
Applicant
Edward Weck, Inc.
Mchenry, IL, US
Received
April 16, 1984
Decision date
August 14, 1984
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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K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsFZP · Traditional Teleflex Medical07/03/2025SE
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

More from Ethicon Endo Surgery, LLC

510(k)DeviceDecision
K915378Weck TrocarHET · Traditional 06/29/1992SE
K914690LM15(TM), Catalog Number - 523821GCJ · Traditional 03/23/1992SE
K911915Hemoclip IIFZP · Traditional 01/09/1992SE
K914470Pneumo-Seal(Tm)GCJ · Traditional 11/29/1991SE
K911272Endoscopic Needlholder Cat. Number 114705FHG · Traditional 07/02/1991SE
K902108Hem-O-Lok(Tm)FZP · Traditional 08/06/1990SE
K902232Weck Electrosurgical Generator #174200GEI · Traditional 08/02/1990SE
K897045Bowie-Dick Test Card Catalog Number 008018JOJ · Traditional 02/15/1990SE
K871110Coronary Artery Bypass Graft (Cabg) MarkerDSY · Traditional 08/27/1987SE
K851251Auto/Manual Titanium Hemoclip Ligating Clip 527200FZP · Traditional 07/02/1985SE

Questions and answers

When was Hemoclip Ligating Clips M/Large cleared by the FDA?

Hemoclip Ligating Clips M/Large (K841548) received a 510(k) decision of Substantially Equivalent on August 14, 1984, 120 days after the submission was received.

What is the product code of K841548?

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