FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

EPR-200 PROGRAMMER MODEL 010

K Number: K800376 · Decision Apr 21, 1980
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
24
Applicant Total
41
Review Days
60

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Basic Information

Device Name
EPR-200 PROGRAMMER MODEL 010
K Number
K800376
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Biotronik Sales, Inc.
Date Received
February 21, 1980
Decision Date
April 21, 1980
Product Code
KRG
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
KRG Programmer, Pacemaker

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Other Clearances by Biotronik Sales, Inc.

K Number Device Name
K875199 NP BIPOLAR ENDOCARDIAL LEAD W/VS-1 CONNECTOR
K853194 ERA-20
K860036 EDP-20 PACEMAKER
K863879 NEOS-M VS-1 PULSE GENERATOR
K863878 TRIOS-M VS-1 PULSE GENERATOR
K863480 BIOTRONIK PERMANENT PACEMAKER ELECTRODE
K860921 NEOS VS-1, PULSE GENERATOR
K860922 MIKROS, MIKROS VS-1, PULSE GENERATOR
K853567 DJP UNIPOLAR
K853566 DJ UNIPOLAR
Search all 41 clearances from Biotronik Sales, Inc. →