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

PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR

K Number: K850651 · Decision Apr 1, 1985
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
460
Applicant Total
96
Review Days
41

Basic Information

Device Name
PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR
K Number
K850651
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
PACESETTER SYSTEMS
Date Received
February 19, 1985
Decision Date
April 1, 1985
Product Code
DXY
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
DXY Implantable Pacemaker Pulse-Generator

Similar 510(k) Clearances

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

View all

Other Clearances by PACESETTER SYSTEMS

K Number Device Name
K910924 ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONE
K902147 ENDOCARDIAL SCREW-IN LEAD MODEL 1028T
K900512 SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS
K900550 FAST-PASS ACE MODELS 1212T/1222T/1216T/1226T
K895447 ENDOCARDIAL SCREW-IN LEAD MODEL 1020T
K891905 CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
K885267 VS-1 MODEL NUMBER 251K PULSE GENERATOR
K890547 SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS
K884733 AFP MODEL 262T PULSE GENERATOR
K883087 PROLOG MP 658M PULSE GENERATOR
Search all 96 clearances from PACESETTER SYSTEMS →