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

VASOSCREEN IMPEDANCE PLETHYSMOGRAPH

K Number: K851102 · Decision May 16, 1985
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
18
Review Days
58

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Basic Information

Device Name
VASOSCREEN IMPEDANCE PLETHYSMOGRAPH
K Number
K851102
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2750
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Sonicaid, Inc.
Date Received
March 19, 1985
Decision Date
May 16, 1985
Product Code
DQB
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
DQB Phlebograph, Impedance

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Other Clearances by Sonicaid, Inc.

K Number Device Name
K873673 BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
K872074 5 MHZ TRANSDUCER
K863803 VASOPULSE(TM)/MODEL 5000
K862720 VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES
K861237 VASOVIEW DUPLEX IMAGING SYSTEM
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. →