FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇷 Türkiye

Avicenna Roboflex

K Number: K233700 · Decision Aug 16, 2024
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
1
Review Days
273

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Basic Information

Device Name
Avicenna Roboflex
K Number
K233700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Elmed Elektronik VE Medikal Sanayi VE Ticaret Anonim Sirketi
Date Received
November 17, 2023
Decision Date
August 16, 2024
Product Code
FGB
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
FGB Ureteroscope And Accessories, Flexible/Rigid

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