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

SIEMENS SIRECUST 732, PATIENT MONITOR

K Number: K901771 · Decision May 30, 1990
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
15
Review Days
41

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Basic Information

Device Name
SIEMENS SIRECUST 732, PATIENT MONITOR
K Number
K901771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Siemens Medical Electronics
Date Received
April 19, 1990
Decision Date
May 30, 1990
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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