Cleared Traditional

Embrella Endoscopic Distal Attachment

K190030 · Micro-Tech (Nanjing) Co., Ltd. · Gastroenterology & Urology
Mar 2019
Decision
57d
Days
Class 2
Risk

About This 510(k) Submission

K190030 is an FDA 510(k) clearance for the Embrella Endoscopic Distal Attachment, a Endoscopic Access Overtube, Gastroenterology-urology (Class II — Special Controls, product code FED), submitted by Micro-Tech (Nanjing) Co., Ltd. (Nanjing, CN). The FDA issued a Cleared decision on March 5, 2019, 57 days after receiving the submission on January 7, 2019. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K190030 FDA.gov
FDA Decision Cleared SESE
Date Received January 07, 2019
Decision Date March 05, 2019
Days to Decision 57 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FED — Endoscopic Access Overtube, Gastroenterology-urology
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation.

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