FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

EMERGENCY CART

K Number: K772320 · Decision Jan 3, 1978
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
7
Applicant Total
80
Review Days
15

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Basic Information

Device Name
EMERGENCY CART
K Number
K772320
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6175
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Physio-Control Corp.
Date Received
December 19, 1977
Decision Date
January 3, 1978
Product Code
BZN
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BZN Cart, Emergency, Cardiopulmonary (Excluding Equipment)

Similar 510(k) Clearances

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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. →