Weck Auto Endo5 5mm Automatic Endoscopic 35cm Applier (AE05ML)

FDA 510(k) K230480 · Teleflex Medical

Substantially Equivalent

510(k) numberK230480

Submission

Device name
Weck Auto Endo5 5mm Automatic Endoscopic 35cm Applier (AE05ML)
Applicant
Teleflex Medical
Morrisville, NC, US
Received
February 22, 2023
Decision date
April 28, 2023
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

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 07/03/2025SE
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K233713Pilling Tracheostomy TubesBTO · Traditional 03/22/2024SE
K232970Hem-o-lok® Ligating ClipsFZP · Traditional 01/12/2024SE
K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen…BSO · Traditional 08/30/2023SE
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Questions and answers

When was Weck Auto Endo5 5mm Automatic Endoscopic 35cm Applier (AE05ML) cleared by the FDA?

Weck Auto Endo5 5mm Automatic Endoscopic 35cm Applier (AE05ML) (K230480) received a 510(k) decision of Substantially Equivalent on April 28, 2023, 65 days after the submission was received.

What is the product code of K230480?

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