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

BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL

K Number: K873673 · Decision Feb 26, 1988
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
47
Applicant Total
18
Review Days
168

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Basic Information

Device Name
BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL
K Number
K873673
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Sonicaid, Inc.
Date Received
September 11, 1987
Decision Date
February 26, 1988
Product Code
DPT
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
DPT Probe, Blood-Flow, Extravascular

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Other Clearances by Sonicaid, Inc.

K Number Device Name
K872074 5 MHZ TRANSDUCER
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. →