FDA 510(k) Substantially Equivalent 🇺🇸 United States

E350I ELECTROCARDIOGRAPH

K Number: K914969 · Decision Mar 26, 1992
Classifications
0
FEI Numbers
11
Registration Numbers
11
Same Product Code
82
Applicant Total
7
Review Days
142

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
E350I ELECTROCARDIOGRAPH
K Number
K914969
Clearance Type
Traditional
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Burdick, Inc.
Date Received
November 5, 1991
Decision Date
March 26, 1992
Product Code
LOS
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LOS), ordered by most recent decision date.

Other Clearances by Siemens Burdick, Inc.

K Number Device Name
K915327 ELITE II ELECTROCARDIOGRAPH,MODIFIED
K915225 MEGACART
K915202 INTERNAL MODEM FOR THE E560 ELECTROCARDIOGRAPH
K913518 TA620 TREADMILL CONTROLLER
K910634 DC200 DEFIBRILLATOR
K910867 T600 TREADMILL