510(k) K993269

IQ NASAL MASK, MODEL P/N 50160 by Sleepnet Corporation — Product Code BZD

K993269 is an FDA 510(k) premarket notification submitted by Sleepnet Corporation for the device "IQ NASAL MASK, MODEL P/N 50160". The FDA issued a decision of Substantially Equivalent on October 27, 1999. The device falls under product code BZD (Ventilator, Non-Continuous (Respirator)), a Class II device regulated under 21 CFR 868.5905. Sleepnet Corporation has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1999
Date Received
September 30, 1999
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Non-Continuous (Respirator)
Device Class
Class II
Regulation Number
868.5905
Review Panel
AN
Submission Type