|  ControlTek works with leading medical companies to develop and deploy FDA-approved medical electronic devices. Our design process meets FDA requirements and supports 510k provisions.
ControlTek works with medical customers in developing the electronic device and PCB requirements (including research and development efforts), hazard analysis, determining the acceptance criteria (including verification & validation efforts), design (circuit, mechanical, PCB layout, firmware, software, etc.), prototyping, testing, documentation, and production support.
Lean more about our Electronic Manufacturing for Medical Devices capabilities by reading our RS Medical - Neuromuscular Stimulator case study.
You can also read our medical devices brochure.
Control Tek is a 13485 certified and FDA Registered Facility.
 |
