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

VSM-1 PHYSIOLOGICAL MONITOR

K Number: K800492 · Decision Mar 18, 1980
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
80
Review Days
14

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Basic Information

Device Name
VSM-1 PHYSIOLOGICAL MONITOR
K Number
K800492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Physio-Control Corp.
Date Received
March 4, 1980
Decision Date
March 18, 1980
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Physio-Control Corp.

K Number Device Name
K991910 LIFEPAK 12 BIPHASIC
K990338 NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM
K983393 LIFEPAK 500 BIPHASIC
K973486 LIFE PAK 12
K962359 LIFEPAK 300
K955854 LIFEPAK 500
K953204 PEDIATRIC QUIK-COMBO
K951593 LIFEPAK 11
K945511 LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER, AND LIFEPAK 11 CARDIAC MONITOR
K943301 QUIK COMBO
Search all 80 clearances from Physio-Control Corp. →