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

CARDIAC PERFORMANCE MONITOR

K Number: K864583 · Decision May 11, 1987
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
11
Review Days
172

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Basic Information

Device Name
CARDIAC PERFORMANCE MONITOR
K Number
K864583
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Vascular Technology Incorporated
Date Received
November 20, 1986
Decision Date
May 11, 1987
Product Code
DQK
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
DQK Computer, Diagnostic, Programmable

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Other Clearances by Vascular Technology Incorporated

K Number Device Name
K082870 VTI INTRAOPERATIVE DOPPLER SYSTEMS
K031091 VTI 20 MHZ GATED DOPPLER
K002990 VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001
K944764 VTI DISPOSABLE PRESSURE DISPLAY SET
K922738 VTI OXYGEN ANALYZER
K890058 VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM
K883960 GIPHY MONITOR
K862114 KHURI REGIONAL TISSUE PH MONITOR
K862113 NO. 100352 GALVANIC OXYGEN SENSOR
K852275 VASCULAR TECH # 100123 POLAROGRAPHIC OXGYEN SENSOR
Search all 11 clearances from Vascular Technology Incorporated →