This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Device | PROGRAMALITH(TM) MODEL 223 PULSE GENERATOR & 398 P |
Generic Name | Implantable Pulse Generator, Pacemaker (non-crt) |
Applicant | PACESETTER SYSTEMS |
Date Received | 1983-06-06 |
Decision Date | 1983-08-10 |
PMA | P820023 |
Supplement | S003 |
Product Code | LWP |
Advisory Committee | Cardiovascular |
Expedited Review | No |
Combination Product | No |
Applicant Address | PACESETTER SYSTEMS 12884 Bradley Ave. sylmar, CA 91342 |
Supplement Number | Date | Supplement Type |
---|---|---|
P820023 | Original Filing | |
S005 | 1983-11-03 | |
S004 | 1983-08-09 | |
S003 | 1983-06-06 | |
S002 | 1983-03-25 | |
S001 |