Atlas FDA

EKG SPEAKS

FDA 510(k) clearance K032926 · decided 2003-10-15

Clearance details

K-number
K032926
Device name
EKG SPEAKS
Applicant
Medtronic Vascular
Decision
Substantially Equivalent
Date received
2003-09-22
Decision date
2003-10-15
Days to decision
23 days
Clearance type
Special
Product code
KRE
Device class
2
Regulation number
870.3640
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Minneapolis, MN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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PACEART OPTIMA SYSTEM SOFTWARE (K110693)Medtronic, Inc.2011-06-08
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PACEMAKER FUNCTION ANALYZER (K870909)Paceart, Inc.1987-04-27
PACEMAKER SYS ANALYZER #384 (K833647)Pacesetter Systems1983-12-16
PACEMAKER SYS. ANALYZER 378 (K832959)Siemens Elema AB1983-11-14
CARDIOMEMO (K803286)Instromedix, Inc.1981-03-17
ELECTRONIC PACEMAKER WAVEFORM ANALYZER (K800696)Instromedix, Inc.1980-08-14
ULTRA-CHEK PACEMAKER MONITOR (K801022)Powers Medical Systmes1980-06-17
PACE-PULSE/COMPUTRAC (K800782)Bib, Inc.1980-05-28

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Resolute Onyx Zotarolimus-Eluting Coronary Stent System - RX and OTW; Onyx Frontier Zotarolimus-Eluting Coronary Stent S (P160043/S089)Medtronic Vascular2025-12-19
Endurant II/IIs Stent Graft System (P100021/S131)Medtronic Vascular2025-10-23
Endurant Stent Graft System, Endurant II Stent Graft System, Endurant IIs Stent Graft System (P100021/S129)Medtronic Vascular2025-09-15
Resolute Onyx (P160043/S088)Medtronic Vascular2025-06-26
Endurant Stent Graft System (P100021/S130)Medtronic Vascular2025-06-12
Valiant Thoracic Stent Graft with the Captivia Delivery System (P100040/S073)Medtronic Vascular2025-06-12
Valiant Thoracic Stent Graft with the Captivia Delivery System (P100040/S072)Medtronic Vascular2025-05-20
Valiant Thoracic Stent Graft with the Captiva Delivery System (P100040/S069)Medtronic Vascular2025-05-08