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

5 MHZ TRANSDUCER

K Number: K872074 · Decision Aug 25, 1987
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
18
Review Days
88

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Basic Information

Device Name
5 MHZ TRANSDUCER
K Number
K872074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Sonicaid, Inc.
Date Received
May 29, 1987
Decision Date
August 25, 1987
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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Other Clearances by Sonicaid, Inc.

K Number Device Name
K873673 BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
K863803 VASOPULSE(TM)/MODEL 5000
K862720 VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES
K861237 VASOVIEW DUPLEX IMAGING SYSTEM
K851102 VASOSCREEN IMPEDANCE PLETHYSMOGRAPH
K833902 VASOSCAN
K832374 PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH
K833488 SONICOMP
K833227 SONICAID MODEL D206E AIR EMBOLI-DETECT
K831371 MODEL FM5
Search all 18 clearances from Sonicaid, Inc. →