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

PRESSURE MONITOR MANOMETRIC SYS.

K Number: K771265 · Decision Nov 22, 1977
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
30
Applicant Total
80
Review Days
132

Basic Information

Device Name
PRESSURE MONITOR MANOMETRIC SYS.
K Number
K771265
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1725
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
PHYSIO-CONTROL CORP.
Date Received
July 13, 1977
Decision Date
November 22, 1977
Product Code
KLA
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube

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K Number Device Name
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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
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