Gemscom Series 6000, Models 6100, 6200 & 6300
FDA 510(k) K940009 · General Devices
510(k) numberK940009
Submission
- Device name
- Gemscom Series 6000, Models 6100, 6200 & 6300
- Applicant
- General Devices
Ridgefield, NJ, US - Received
- January 4, 1994
- Decision date
- April 14, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2910
- Specialty
- Cardiovascular
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| K243837 | iBSMDRG · Traditional | Iorbit Digital Technologies Private Limited | 05/16/2025SE |
| K242018 | UbiqVue 2A Multi-parameter System (UX2550)DRG · Traditional | Lifesignals, Inc. | 11/12/2024SE |
| K241101 | BioButton SystemDRG · Traditional | Biointellisense, Inc. | 09/26/2024SE |
| K240251 | ANNE ChestDRG · Traditional | Sibel Health, Inc. | 06/03/2024SE |
| K223711 | ANNE OneDRG · Traditional | Sibel Health, Inc. | 08/10/2023SE |
| K220526 | HD+12, HD+15DRG · Traditional | Cardioline S.P.A | 05/15/2023SE |
More from Cardioline S.P.A
| 510(k) | Device | Decision |
|---|---|---|
| K013533 | EMS Telemedicine Option (for Gems Series 4000)DRG · Traditional | 01/18/2002SE |
| K002089 | Rosetta-Lt/Rosetta-RxDRG · Traditional | 11/21/2000SE |
| K993202 | EIM-107 Prep-CheckGZO · Traditional | 12/17/1999SE |
| K935839 | Gemscom Series 5000,DRG · Traditional | 11/10/1994SE |
| K921929 | Gemscom Series 300 12-LEAD ECG (12-LEAD Option)DXH · Traditional | 09/18/1992SE |
| K914889 | Gemscom Series 3000DRG · Traditional | 03/04/1992SE |
| K912008 | Tru-View Multi-Channel DisplayDRT · Traditional | 10/09/1991SE |
| K896153 | Modified DR-2C/PMC 100DSH · Traditional | 01/19/1990SE |
| K862596 | DR-2C (Modification)DSF · Traditional | 09/26/1986SE |
| K844650 | DR-2CDXJ · Traditional | 01/22/1985SE |
Questions and answers
When was Gemscom Series 6000, Models 6100, 6200 & 6300 cleared by the FDA?
Gemscom Series 6000, Models 6100, 6200 & 6300 (K940009) received a 510(k) decision of Substantially Equivalent on April 14, 1995, 465 days after the submission was received.
What is the product code of K940009?
The FDA product code is DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency, a Class II (moderate risk) device regulated under 21 CFR 870.2910.