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

CARDIAC SECTOR PROBE 3.5. MHZ

K Number: K850145 · Decision Apr 10, 1985
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
71
Applicant Total
519
Review Days
86

Basic Information

Device Name
CARDIAC SECTOR PROBE 3.5. MHZ
K Number
K850145
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Date Received
January 14, 1985
Decision Date
April 10, 1985
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOP Transducer, Ultrasonic

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