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

SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A

K Number: K844791 · Decision Apr 10, 1985
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
395
Applicant Total
32
Review Days
121

Basic Information

Device Name
SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A
K Number
K844791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
ANALOGIC CORP.
Date Received
December 10, 1984
Decision Date
April 10, 1985
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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