IQ NASAL MASK, MODEL P/N 50160

About This 510(k) Submission

K993269 is an FDA 510(k) clearance for the IQ NASAL MASK, MODEL P/N 50160, a Ventilator, Non-continuous (respirator) (Class II — Special Controls, product code BZD), submitted by Sleepnet Corporation (Manchester, US). The FDA issued a Cleared decision on October 27, 1999, 27 days after receiving the submission on September 30, 1999. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5905.