FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)

K Number: K082667 · Decision Oct 30, 2008
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
13
Review Days
48

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)
K Number
K082667
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Visionsense, Ltd.
Date Received
September 12, 2008
Decision Date
October 30, 2008
Product Code
EOB
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EOB Nasopharyngoscope (Flexible Or Rigid)

Similar 510(k) Clearances

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

View all

Other Clearances by Visionsense, Ltd.

K Number Device Name
K223020 VS3-Iridium System (VS3-IR)
K210265 VS3 Iridium Sytem
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
Search all 13 clearances from Visionsense, Ltd. →