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Fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also please note the regulation entitled Misbranding by reference to premarket notification 21 CFR Part 807. Zuckerman M. D. Director Division of Cardiovascular Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure Indications for Use Form Approved OMB No. 0910-0120 Expiration Date January 31 2017 See PRA Statement below. 510 k Number if known Device Name AirStrip One Web Client information is...
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Airstrip Technologies Inc is a technology company that specializes in developing software solutions for the healthcare industry.
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