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

VS3 Iridium Sytem

K Number: K210265 · Decision Nov 22, 2021
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
60
Applicant Total
13
Review Days
294

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Basic Information

Device Name
VS3 Iridium Sytem
K Number
K210265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visionsense, Ltd.
Date Received
February 1, 2021
Decision Date
November 22, 2021
Product Code
OWN
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
OWN Confocal Optical Imaging

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OWN), 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)
K171208 Trans-anal Introducer
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. →