Bear Hugger Warming Device. Under the 510 k program the fda can clear a medical device without clinical proof that it is safe if it is similar enough to a previous device already on the market. The bair hugger faw forced air warming surgical device may be to blame for major joint infections after hip and knee replacement surgeries. The bair hugger was produced by arizant previously known as augustine medicine.
The bair hugger faw forced air warming surgical device may be to blame for major joint infections after hip and knee replacement surgeries. Is battling lawsuits from more than 50 orthopedic surgery patients who say the company s popular bair hugger warming blankets used to keep people warm before surgery circulated.
The bair hugger system received fda clearance in 1987.
The bair hugger was produced by arizant previously known as augustine medicine. The bair hugger system is the most used and studied method of surgical warming in the country with its clinical benefits efficacy and safety well documented in over 170 studies and more than 60 randomized controlled clinical trials. Is battling lawsuits from more than 50 orthopedic surgery patients who say the company s popular bair hugger warming blankets used to keep people warm before surgery circulated. The bair hugger was produced by arizant previously known as augustine medicine.
