FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Trans-anal Introducer

K Number: K171208 · Decision Feb 5, 2018
Classifications
1
FEI Numbers
116
Registration Numbers
116
Same Product Code
100
Applicant Total
13
Review Days
286

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Basic Information

Device Name
Trans-anal Introducer
K Number
K171208
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Visionsense, Ltd.
Date Received
April 25, 2017
Decision Date
February 5, 2018
Product Code
FED
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FED Endoscopic Access Overtube, Gastroenterology-Urology

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FED), ordered by most recent decision date.

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Other Clearances by Visionsense, Ltd.

K Number Device Name
K223020 VS3-Iridium System (VS3-IR)
K210265 VS3 Iridium Sytem
K153548 VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
K152204 VS3-IR system
K150018 VS3-IR-MMS System
K141002 VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
K131434 VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
K123467 VS3
K082355 VISIONSENSE STEREOSCOPIC VISION SYSTEM
K082667 VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)
Search all 13 clearances from Visionsense, Ltd. →