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

OLYMPUS UM-S30-25R ULTRASONIC PROBE AND ASSOCIATED ANCILLARY EQUIPMENT FOR URINARY USE

K Number: K994069 · Decision Jun 2, 2000
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
149
Review Days
183

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Basic Information

Device Name
OLYMPUS UM-S30-25R ULTRASONIC PROBE AND ASSOCIATED ANCILLARY EQUIPMENT FOR URINARY USE
K Number
K994069
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Olympus America, Inc.
Date Received
December 2, 1999
Decision Date
June 2, 2000
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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