510(k) K241469

iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask by Sleepnet Corporation — Product Code BZD

K241469 is an FDA 510(k) premarket notification submitted by Sleepnet Corporation for the device "iQ 2 Nasal Vented Mask; Phantom 2 Nasal Vented Mask". The FDA issued a decision of Substantially Equivalent on June 15, 2024. 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
June 15, 2024
Date Received
May 24, 2024
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