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

FLEXIBLE URETEROSCOPE

K Number: K872282 · Decision Sep 14, 1987
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
112
Applicant Total
14
Review Days
90

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Basic Information

Device Name
FLEXIBLE URETEROSCOPE
K Number
K872282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Intramed Laboratories, Inc.
Date Received
June 16, 1987
Decision Date
September 14, 1987
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

Similar 510(k) Clearances

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Other Clearances by Intramed Laboratories, Inc.

K Number Device Name
K953258 TITANIUM HEMOSTATIC CLIP
K942457 GRAFT THROMBECTOMY INSTRUMENTS
K931792 ARTHROSCOPE
K925283 VALVULOTOME
K934696 ANGIOSCOPE
K922114 ENDOSCOPIC RETRIEVAL BASKET
K914385 OPTICAL VALVULOTOME
K904465 FLEXIBLE ARTHROSCOPE
K903528 LAPAROSCOPE
K902444 CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
Search all 14 clearances from Intramed Laboratories, Inc. →