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Rapid Reboot Recovery Products, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2020-12-22
TypeNumberDevice NameCodeDateActions
510(k) K203552 Rapid RebootIRP2020-12-22 View
510(k) K182668 Rapid Reboot Compression Therapy SystemIRP2018-12-14 View
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