Dr. Eric Edward Haeger, age 57, of Brewster, Wash., has pleaded guilty to adulterating and misbranding CPAP and BiPAP devices with the intent to defraud or mislead, according to the U.S. Attorney's ...
GlobalData on MSN
FDA clears SleepRes’ Kricket PAP device for obstructive sleep apnoea
The FDA has granted 510(k) clearance to SleepRes’ KPAP-powered Kricket PAP device for the treatment of obstructive sleep ...
A physician from Brewster, has pleaded guilty to charges of adulterating and misbranding medical devices with the intent to ...
SleepRes announced today that it received FDA 510(k) clearance for its Kricket PAP device for treating obstructive sleep ...
KPAP™ sleep therapy platform is designed to enable a more comfortable, adaptive, and patient-centered alternative to ...
Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...
Cruise West Coast on MSN
Cruising with sleep apnea: What you need to know before bringing your CPAP on a cruise
Cruising with a CPAP machine is straightforward when you know each cruise line's specific policies and pack the right ...
The U.S. Attorney's Office says an eastern Washington doctor pled guilty to augmenting recalled medical devices to sell them ...
A Brewster physician who operates a sleep diagnostic clinic in Moses Lake and Wenatchee will be sentenced March 24 as part of ...
The FDA’s oversight of medical device recalls continues to be plagued by staffing challenges—forcing some activities to be ...
SleepRes, Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the Kricket PAP device, powered by Kairos Positive Airway Pressure (KPAP), for the treatment ...
13don MSN
The FDA Rarely Forces Manufacturers to Recall Dangerous Medical Devices, Watchdog Report Finds
Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...
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