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

ACUTE CARDIAC CARE SYSTEM

K Number: K772006 · Decision Nov 28, 1977
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
334
Applicant Total
80
Review Days
38

Basic Information

Device Name
ACUTE CARDIAC CARE SYSTEM
K Number
K772006
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
PHYSIO-CONTROL CORP.
Date Received
October 21, 1977
Decision Date
November 28, 1977
Product Code
DRT
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
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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K Number Device Name
K991910 LIFEPAK 12 BIPHASIC
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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. →