Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7

FDA 510(k) K061324 · Rtc Inc.-Memcath Technologies, LLC

Substantially Equivalent

510(k) numberK061324

Submission

Device name
Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7
Applicant
Rtc Inc.-Memcath Technologies, LLC
West St. Paul, MN, US
Received
May 11, 2006
Decision date
June 20, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FED – Endoscopic Access Overtube, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To facilitate passage and aid advancement of endoscopes into the body, especially in cases of repeated intubation.

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K260965CVAC Aspiration SystemFED · Special Calyxo, Inc.04/13/2026SE
K260521ClearEVAC Ureteral Aspirating Access Sheath (PUS-100-1040,PUS-100-1050…FED · Traditional Zhuhai Pusen Medical Technology Co., Ltd.04/06/2026SE
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K250128Single Use Suction-Evacuation Ureteral Access SheathFED · Traditional Anhui Happiness Workshop Medical Instruments…09/19/2025SE
K250132Ureteral Access SheathFED · Traditional Zhejiang YiGao Medical Technology Co., Ltd.09/05/2025SE
K250695Single-use Ureteral Access SheathFED · Traditional Shenzhen HugeMed Medical Technical Development…07/08/2025SE
K251599Single-use Ureteral Access SheathFED · Special Hunan Vathin Medical Instrument Co., Ltd.07/03/2025SE
K250585LumenaTM Ureteral Access SheathFED · Traditional Cathegenix (Xiamen) Co., Ltd.06/27/2025SE

More from Cathegenix (Xiamen) Co., Ltd.

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K061663Endomedical Technologies Quik-Cover Flexible Endoscope Barrier Sheath for…EOB · Traditional 09/06/2006SE

Questions and answers

When was Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7 cleared by the FDA?

Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7 (K061324) received a 510(k) decision of Substantially Equivalent on June 20, 2006, 40 days after the submission was received.

What is the product code of K061324?

The FDA product code is FED – Endoscopic Access Overtube, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.