510(k) K233013

Device
2-Way 100% Silicone Cleartract Catheter
Applicant
Silq Technologies Corporation
510(k) number
K233013
Product code
EZL
Decision
Substantially Equivalent (SESE)
Decision date
2024-01-23
Date received
2023-09-22
Regulation
876.5130
Classification name
Catheter, Retention Type, Balloon
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
D. Verne Sharma
Address
323 Sunny Isles Blvd. Sunny Isles Beach FL US 33160 33160

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code EZL

510(k)DeviceApplicantDecision date
K252537Rusch SoftSimplastic Foley CathetersTeleflex Medical Sdn. Bhd.2026-01-20
K243011Silicone Urethral Catheter (Silicone Urethral Catheter)Guangdong Ecan Medical Co., Ltd.2025-06-16
K241424InnoCare Specialty Foley CatheterInnocare Urologics, LLC2024-09-18
K232469RĂ¼sch Latex Gold Foley CatheterTeleflexmedical, Inc.2024-08-01
K240057TraumaGuard Intra-abdominal Pressure Sensing SystemSentinel Medical Technologies, LLC2024-04-17
K233411Folysil Silicone CatheterColoplast Corp.2024-04-15
K212077Teleflex Rusch SoftSimplastic Foley CathetersTeleflexmedical, Inc.2023-07-27
K231101Flume CatheterFlume Catheter Company, Ltd.2023-06-29
K221020Accuryn Monitoring System, Accuryn SmartFoley IAP UO Temp Tray System 12 F, Accuryn SmartFoley IAP UO Temp Tray System 14 FPotrero Medical, Inc.2023-01-13
K2221182-Way 100% Silicone Cleartract CatheterSilq Technologies, Corp.2022-12-01
K2216252-Way 100% Silicone ClearTract CatheterSilq Technologies Corporation2022-07-01
K212151FLUME catheterThe Flume Catheter Company, Ltd.2021-11-03
K202134Well Lead All Silicone Foley Catheter with Temperature SensorWell Lead Medical Co., Ltd.2021-04-08
K201776Foley Balloon Catheter for UrologyApollon Co., Ltd.2020-12-30
K202698Prefilled SyringeHangzhou Primecare Medical Co., Ltd.2020-12-15