Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

angioLOCK Polymer Ligating Clip

K-Number: K220006 · 2022-03-02

ApplicantA2 Medical Systems, LLC
Decision Date2022-03-02
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

angioLOCK Polymer Ligating Clip is a medical device manufactured by A2 Medical Systems, LLC. It received FDA 510(k) clearance on 2022-03-02 under approval number K220006. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the angioLOCK Polymer Ligating Clip?

angioLOCK Polymer Ligating Clip is a medical device that received FDA 510(k) clearance on 2022-03-02. It is manufactured by A2 Medical Systems, LLC. The 510(k) number is K220006.

When was angioLOCK Polymer Ligating Clip approved by the FDA?

angioLOCK Polymer Ligating Clip received FDA 510(k) clearance on 2022-03-02, under approval number K220006.

What company makes angioLOCK Polymer Ligating Clip?

angioLOCK Polymer Ligating Clip is manufactured by A2 Medical Systems, LLC.

What is the FDA product code for angioLOCK Polymer Ligating Clip?

The FDA product code for angioLOCK Polymer Ligating Clip is FZP.

Related Clinical Trials

NCT06364865 AE05ML Device for ML Hem-o-lok Polymer Clip Delivery in Laparoscopic Surgical Procedures Observational Registery Study COMPLETED

Other Devices by A2 Medical Systems, LLC

K230966angiOCCLUDE Ligating Clips

Related Devices (Code: FZP)

K161758Weck Auto Endo10 Automatic Endoscopic Clip ApplierTeleflex Medical K151943Vas-Q-ClipNanova Biomaterials, Inc. K160454AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove ClipAtriCure, Inc. K152082Vesocclude Polymer Ligating ClipVesocclude Medical, LLC K153500AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove PRO V ClipAtriCure, Inc. K173031AtriClip LAA Exclusion System with Preloaded PRO·V ClipAtriCure, Inc.

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.

↑