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

PENTAX URETERORENOFIBERSCOPE, MODEL FUR-10P

K Number: K914106 · Decision Jan 10, 1992
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
67
Review Days
119

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Basic Information

Device Name
PENTAX URETERORENOFIBERSCOPE, MODEL FUR-10P
K Number
K914106
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pentax Precision Instrument Corp.
Date Received
September 13, 1991
Decision Date
January 10, 1992
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 Pentax Precision Instrument Corp.

K Number Device Name
K041396 FG-36UX FIBER ULTRASOUND GASTROSCOPE
K041395 EG-3630UR
K041397 EG-3830UT
K031789 EG-3830UT, VIDEO ULTRASOUND GASTROSCOPE
K023401 EG-3830UT, VIDEO ULTRASOUND GASTROSCOPE
K023376 EB-1830T3, VIDEO BRONCHOSCOPE
K021276 FG-36UX FIBER ULTRASOUND GASTROSCOPE
K021278 EG-3630UR, ULTRASOUND VIDEO GASTROSCOPE
K013640 EG-3630UR, ULTRASUND VIDEO GASTROSCOPE
K010740 FG-36UX, FIBER ULTRASOUND GASTROSCOPE
Search all 67 clearances from Pentax Precision Instrument Corp. →