Atlas FDA

CORDIS SEQUICOR THETA MODELS 233D & 233E

FDA premarket approval P820014/S020 · decided 1985-12-30

Approval details

PMA number
P820014
Supplement
S020
Trade name
CORDIS SEQUICOR THETA MODELS 233D & 233E
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Telectronics Pacing Systems, Inc.
Date received
1985-08-09
Decision date
1985-12-30
Days to decision
143 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Englewood, CO

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510(k) clearances by this applicant

RecordFirmDate
MAXIM PF MODELS 033-581/033-590 (K961118)Telectronics Pacing Systems, Inc.1996-07-15
STERILIZATION (K943657)Telectronics Pacing Systems, Inc.1996-06-24
BIFURCATED LEAD ADAPTORS, 3.2MM & 5.0 MM (K934899)Telectronics Pacing Systems, Inc.1994-05-12
NEW LEAD INTRODUCER KITS, VARIOUS MODELS (K926340)Telectronics Pacing Systems, Inc.1993-05-27
NEW EXTRUSION VENDOR FOR POLYURETHANE TUBING (K914489)Telectronics Pacing Systems, Inc.1992-08-17
UNIVERSAL TERMINAL CAP, 3.2MM (K913919)Telectronics Pacing Systems, Inc.1991-12-31
UNIPOLAR UPSIZING ADAPTOR (K912773)Telectronics Pacing Systems, Inc.1991-10-23
100 CM PERMANENT PACING LEAD MODELS (K911273)Telectronics Pacing Systems, Inc.1991-08-28