Mist Endoscopic Needles

FDA 510(k) K951648 · Mist, Inc.

Substantially Equivalent

510(k) numberK951648

Submission

Device name
Mist Endoscopic Needles
Applicant
Mist, Inc.
Great Neck, NY, US
Received
April 10, 1995
Decision date
May 12, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBK – Endoscopic Injection Needle, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.

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K240675Endoscopic Injection NeedlesFBK · Traditional Promisemed Hangzhou Meditech Co., Ltd.10/04/2024SE
K241523injeTAK Adjustable Tip Needle (DIS199; DIS201)FBK · Special Laborie Medical Technologies, Corp.08/27/2024SE
K232200Disposable Injection NeedlesFBK · Traditional Ningbo Xinwell Medical Technology Co., Ltd.04/12/2024SE
K232826Articulator Injection Needle (00711807), Articulator Injection Needle (00711810)…FBK · Traditional Steris03/08/2024SE
K232442Disposable Endoscope Injection NeedlesFBK · Traditional Zhejiang Soudon Medical Technology Co., Ltd.11/09/2023SE

More from Zhejiang Soudon Medical Technology Co., Ltd.

510(k)DeviceDecision
K970937Mist Micro Interchangeable Scope System (TM)GCJ · Traditional 09/26/1997SE
K971150Mist Panoramic Laparoscope a Rigid LaparoscopeGCJ · Traditional 09/23/1997SE
K952323Mist Electrosurgical Probes, Various Styles & SizesJOS · Traditional 06/23/1995SE
K952290Mist Electrosurgical Probes, Various Styles & Sizes, Surgical Instruments Used During…JOS · Traditional 06/23/1995SE
K951692Mist Endoscopic ProbesGCJ · Traditional 05/03/1995SE
K951481Mist Endoscopic CannulasGCJ · Traditional 05/03/1995SE
K951480Mist TrocarsGCJ · Traditional 05/03/1995SE

Questions and answers

When was Mist Endoscopic Needles cleared by the FDA?

Mist Endoscopic Needles (K951648) received a 510(k) decision of Substantially Equivalent on May 12, 1995, 32 days after the submission was received.

What is the product code of K951648?

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