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

OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12

K Number: K900880 · Decision Apr 29, 1991
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
142
Review Days
427

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Basic Information

Device Name
OLYMPUS JF-UM3-7.5/-12 AND CF-UM3-7.5/-12
K Number
K900880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
February 26, 1990
Decision Date
April 29, 1991
Product Code
ITX
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
ITX Transducer, Ultrasonic, Diagnostic

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K931764 HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES
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K931994 RESECTOSCOPE SHEATH
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K934361 OLYMPUS CREATININE REAGENT
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