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

VASOPULSE(TM)/MODEL 5000

K Number: K863803 · Decision May 6, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
52
Applicant Total
18
Review Days
219

Basic Information

Device Name
VASOPULSE(TM)/MODEL 5000
K Number
K863803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2780
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SONICAID, INC.
Date Received
September 29, 1986
Decision Date
May 6, 1987
Product Code
JOM
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
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

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K Number Device Name
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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
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