Cardiotest 2200
FDA 510(k) K790503 · Cardiac Pacemakers, Inc.
510(k) numberK790503
Submission
- Device name
- Cardiotest 2200
- Applicant
- Cardiac Pacemakers, Inc.
Mchenry, IL, US - Received
- March 13, 1979
- Decision date
- May 17, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DTA – Tester, Pacemaker Electrode Function
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.3720
- Specialty
- Cardiovascular
Other 510(k)s with product code DTA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K163008 | CareLink SmartSync Device Manager - Pacing System AnalyzerDTA · Traditional | Medtronic, Inc. | 02/28/2017SE |
| K101982 | Merlin Psa Patient Cable Ex 3150, Cable Adapter EX3170, M Adapter EX3180DTA · Traditional | St Jude Medical, Crmd | 12/21/2010SE |
| K073230 | Models Era 300 and 3105 Pacing System AnalyzersDTA · Special | Biotronik, Inc. | 12/20/2007SE |
| K050884 | Adapter CableDTA · Traditional | Remington Medical, Inc. | 05/19/2005SE |
| K033613 | Modification to Era 300 Dual Chamber Pacing System AnalyzerDTA · Special | Biotronik, Inc. | 12/08/2003SE |
| K022360 | Era 3000; PA-2 IS-1 Adapter; EK-4-N Pacemaker Test Cable; Era 3000 Charger; Era 3000…DTA · Traditional | Biotronik, Inc. | 01/27/2003SE |
| K933069 | Model EP-2 Clinical StimulatorDTA · Traditional | Ep Medical, Inc. | 10/21/1993SE |
| K812104 | Siemens-Elema Psa 376DTA · Traditional | Siemens Corp. | 12/02/1981SE |
| K791380 | Va 1000DTA · Traditional | Vitatron Medical BV | 09/19/1979SE |
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| K920601 | Astra T2, Astra T4, Astra T6DXY · Traditional | 10/28/1992SE |
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| K900498 | Modified Betatron IV Insulin Infusion SystemLZG · Traditional | 02/23/1990SE |
| K894738 | Model 6888 Lead TunnelerDWS · Traditional | 09/13/1989SE |
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Questions and answers
When was Cardiotest 2200 cleared by the FDA?
Cardiotest 2200 (K790503) received a 510(k) decision of Substantially Equivalent on May 17, 1979, 65 days after the submission was received.
What is the product code of K790503?
The FDA product code is DTA – Tester, Pacemaker Electrode Function, a Class II (moderate risk) device regulated under 21 CFR 870.3720.