CORDIS SEQUICOR THETA MODELS 233D & 233E

Implantable Pulse Generator, Pacemaker (non-crt)

FDA Premarket Approval P820014 S025

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.

Pre-market Approval Supplement Details

DeviceCORDIS SEQUICOR THETA MODELS 233D & 233E
Classification NameImplantable Pulse Generator, Pacemaker (non-crt)
Generic NameImplantable Pulse Generator, Pacemaker (non-crt)
ApplicantTELECTRONICS PACING SYSTEMS, INC.
Date Received1986-03-26
Decision Date1986-05-05
PMAP820014
SupplementS025
Product CodeLWP
Advisory CommitteeCardiovascular
Expedited ReviewNo
Combination Product No
Applicant Address TELECTRONICS PACING SYSTEMS, INC. 7400 South Tucson Way englewood, CO 80112

Supplemental Filings

Supplement NumberDateSupplement Type
P820014Original Filing
S044 1990-04-19 Normal 180 Day Track
S043 1990-01-16 Normal 180 Day Track
S042 1989-11-02 Normal 180 Day Track
S041 1989-04-03 Normal 180 Day Track
S040
S039 1988-11-15 Normal 180 Day Track
S038 1988-06-29 Normal 180 Day Track
S037 1988-06-14 Normal 180 Day Track
S036 1988-05-09 Normal 180 Day Track
S035 1988-02-16 Normal 180 Day Track
S034 1988-02-12 Normal 180 Day Track
S033 1988-01-15 Normal 180 Day Track
S032 1987-08-05 Normal 180 Day Track
S031 1987-03-17 30-Day Supplement
S030 1987-01-21 Special (immediate Track)
S029 1986-12-15 Normal 180 Day Track
S028 1986-10-16 Special (immediate Track)
S027 1986-09-24 Special (immediate Track)
S026 1986-07-11 Normal 180 Day Track
S025 1986-03-26
S024 1986-02-14
S023 1985-12-06
S022 1985-11-20
S021 1985-10-15
S020 1985-08-09
S019 1985-07-12
S018
S017 1985-04-09
S016
S015 1985-02-25
S014 1984-12-31
S013
S012 1984-12-24
S011
S010 1984-10-15
S009 1984-09-10
S008 1984-09-06
S007 1984-01-10
S006 1983-12-08
S005 1983-08-22
S004 1983-04-27
S003 1983-04-21
S002 1982-09-24
S001 1982-03-02

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