510(k) K970497

Device
PACE 101H
Applicant
SULZER OSCOR, INC.
510(k) number
K970497
Product code
DTE  
Decision
Substantially Equivalent (SESE)
Decision date
1997-06-04
Date received
1997-02-10
Regulation
870.3600
Classification name
Pulse-generator, Pacemaker, External
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
MILA DOSKOCIL
Address
3816 Desoto Blvd. Palm Harbor FL US 34683 34683

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Other 510(k) Records For Product Code DTE  

510(k)DeviceApplicantDecision date
K241781Solo Pace ControlSolo Pace, Inc.2025-01-10
K232721Lifetech Cardio Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.2024-01-07
K201011Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.2020-05-13
K190825Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.2019-04-30
K182839Lifetech Cardio Model 8301 Temporary PacemakerShenzhen Lifetech Cardio Medical Electronics Co., Ltd.2019-02-28
K181973Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.2018-08-21
K180873Medtronic Model 53401 External Pulse Generator (EPG)Medtronic, Inc.2018-04-19
K162054Medtronic Temporary External Pacemaker 53401Medtronic, Inc.2016-10-18
K162550Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.2016-10-12
K150246Medtronic Model 5392 External Pulse Generator (EPG)Medtronic, Inc.2015-02-18
K132924MEDTRONIC EXTERNAL PULSE GENERATOR (EPG)Medtronic, Inc.2013-10-31
K123916PSA SERIESOsypka Medical, Inc.2013-04-09
K042708ERA 3000 PACING SYSTEM ANALYZERBiotronik, Inc.2004-10-20
K033130PACE 101/PACE 101H, MODEL 3077 SSI TEMPORARY PULSE GENERATOROsypka Medical, Inc.2003-10-31
K023080GALIX PACESTARGalix Biomedical Instrumentation, Inc.2003-06-11

Legacy Summary

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FDA Review

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