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FDA 510(k)

HEM-O-LOK MODEL NUMBERS 523900, 523970

K-Number: K982941 · 1998-11-19

ApplicantWeck Closure Systems
Decision Date1998-11-19
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEM-O-LOK MODEL NUMBERS 523900, 523970 is the device name listed in this FDA 510(k) record. The listed applicant is Weck Closure Systems. It received FDA 510(k) clearance on 1998-11-19 under 510(k) number K982941. 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 HEM-O-LOK MODEL NUMBERS 523900, 523970?

HEM-O-LOK MODEL NUMBERS 523900, 523970 is a medical device that received FDA 510(k) clearance on 1998-11-19. The listed applicant is Weck Closure Systems. The 510(k) number is K982941.

When did HEM-O-LOK MODEL NUMBERS 523900, 523970 receive FDA 510(k) clearance?

HEM-O-LOK MODEL NUMBERS 523900, 523970 received FDA 510(k) clearance on 1998-11-19, under 510(k) number K982941.

Who is the listed applicant for HEM-O-LOK MODEL NUMBERS 523900, 523970?

The FDA 510(k) record lists Weck Closure Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEM-O-LOK MODEL NUMBERS 523900, 523970?

The FDA product code for HEM-O-LOK MODEL NUMBERS 523900, 523970 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Weck Closure Systems 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.

K011660WECK CARDIAC PACING WIRESK003337HEM-O-LOK SMX, MODEL 544220; HEM-O-LOK ML, MODEL 544230; HEM-O-LOK MLX, MODEL 544240K993157HEM-O-LOK SMX POLYMER CLIPS, MODEL 544220, HEM-0-LOK MLX POLYMER CLIPS, MODEL 544240K982944HEM-O-LOCK, MODEL 523935K982313HORIZON TITANIUM CLIPS, HORIZON TANTALUM CLIPS

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.

K260677Vessel Closure Device (VCD177213P)Vcd Medical S.R.L.K254231Inno-Hook™ Disposable Clip Appliers (Ligating Clips) and Inno-Hook™ Ligating ClipsTaiwan Surgical CorporationK253781InnoClip Clip ApplierTaiwan Surgical CorporationK253903InnoClip Disposable Clip ApplierTaiwan Surgical CorporationK250643Disposable Polymer Ligation ClipsHangzhou Kangji Medical Instrument Co., Ltd.K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsTeleflex Medical

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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