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

SIEMENS CARDIOSTAT 701

K Number: K790794 · Decision May 31, 1979
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
26
Review Days
37

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Basic Information

Device Name
SIEMENS CARDIOSTAT 701
K Number
K790794
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Elmed, Inc.
Date Received
April 24, 1979
Decision Date
May 31, 1979
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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Other Clearances by Elmed, Inc.

K Number Device Name
K010465 DENSTAT
K974793 ELMED ESU 120 M/M DIGITAL
K953271 ELMED RF-ALERT
K952110 ELMED THERMO-FLUX
K926517 ELMED LBC 50-P
K932938 ELMED ESU 300 M/M AND DIGITAL
K921770 ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M
K915731 ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL
K905417 ELMED PNEUMOMAT DIGITAL
K881431 SIEMENS STEREODYNATOR 828
Search all 26 clearances from Elmed, Inc. →