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PROGRAMALITH(TM) MODEL 223 PULSE GENERATOR & 398 P

FDA premarket approval P820023/S002 · decided 1983-05-03

Approval details

PMA number
P820023
Supplement
S002
Trade name
PROGRAMALITH(TM) MODEL 223 PULSE GENERATOR & 398 P
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Pacesetter Systems
Date received
1983-03-25
Decision date
1983-05-03
Days to decision
39 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Sylmar, CA

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510(k) clearances by this applicant

RecordFirmDate
ENDOCARDIAL LEADS-MOD. TO THE POLYVINYLPYRROLIDONE (K910924)Pacesetter Systems1991-08-28
ENDOCARDIAL SCREW-IN LEAD MODEL 1028T (K902147)Pacesetter Systems1990-07-17
SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS (K900512)Pacesetter Systems1990-06-25
FAST-PASS ACE MODELS 1212T/1222T/1216T/1226T (K900550)Pacesetter Systems1990-04-20
ENDOCARDIAL SCREW-IN LEAD MODEL 1020T (K895447)Pacesetter Systems1989-12-20
CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE (K891905)Pacesetter Systems1989-06-05
VS-1 MODEL NUMBER 251K PULSE GENERATOR (K885267)Pacesetter Systems1989-03-28
SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS (K890547)Pacesetter Systems1989-03-22