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

KSEA URETERO-RENO-FIBERSCOPE AND NEPHRO-FIBERSCOPE

K Number: K970427 · Decision Mar 11, 1997
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
35
Review Days
35

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Basic Information

Device Name
KSEA URETERO-RENO-FIBERSCOPE AND NEPHRO-FIBERSCOPE
K Number
K970427
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Karl Storz Endoscopy
Date Received
February 4, 1997
Decision Date
March 11, 1997
Product Code
FGB
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
FGB Ureteroscope And Accessories, Flexible/Rigid

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Other Clearances by Karl Storz Endoscopy

K Number Device Name
K043375 FISCH TITANIUM MIDDLE EAR PROSTHESES
K030848 PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K030009 KSEA POWERSHAVER SYSTEM S2
K023924 AUTOCON II 200 ELECTROSURGICAL GENERATOR
K023187 KSEA SPINOSCOPE
K011700 MODULITH SLK LITHOTRIPTER
K021776 KSEA QUADRO SWITCH
K013107 BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
K011841 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K010569 KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
Search all 35 clearances from Karl Storz Endoscopy →