Atlas FDA

ATA SOFTWARE CARTRIDGE (SWM 1000 I-KTB.0.U)

FDA premarket approval P980023/S010 · decided 2002-08-30

Approval details

PMA number
P980023
Supplement
S010
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ATA SOFTWARE CARTRIDGE (SWM 1000 I-KTB.0.U)
Generic name
TESTER, PACEMAKER ELECTRODE FUNCTION
Applicant
Biotronik, Inc.
Date received
2002-07-22
Decision date
2002-08-30
Days to decision
39 days
Decision code
APPR
Product code
DTA
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR MODIFICATIONS TO THE PCMCIA SOFTWARE CARTRIDGE INCLUDING AN INCREASE IN MEMORY. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME ATA SOFTWARE CARTRIDGE (SWM 1000 I-KTB.0.U) AND IS INTENDED TO ALLOW INTERROGATION AND PROGRAMMING OF BIOTRONIK ICD'S AND PACEMAKERS.

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510(k) clearances by this applicant

RecordFirmDate
BIOMONITOR IV (471155) (K261074)Biotronik, Inc.2026-05-01
Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter (K250706)Biotronik, Inc.2025-04-04
Pantera Pro; Pantera LEO (K242969)Biotronik, Inc.2024-10-25
Selectra 3D Lead Delivery System (443624-443629, 451789-451791); Selectra Slitter Tool (383119); Selectra Accessory Kit (375518) (K240787)Biotronik, Inc.2024-09-12
Oscar Peripheral Multifunctional Catheter system (K241711)Biotronik, Inc.2024-07-11
BIOMONITOR IV (K230375)Biotronik, Inc.2023-05-19
Passeo-35 Xeo Peripheral Dilatation Catheter (K222065)Biotronik, Inc.2023-02-16
BIOMONITOR IIIm, BIOMONITOR III (K221856)Biotronik, Inc.2022-07-27