510(k) K210386

Magneto Nasal Mask by Respironics, Inc. — Product Code BZD

K210386 is an FDA 510(k) premarket notification submitted by Respironics, Inc. for the device "Magneto Nasal Mask". The FDA issued a decision of Substantially Equivalent on July 12, 2021. The device falls under product code BZD (Ventilator, Non-Continuous (Respirator)), a Class II device regulated under 21 CFR 868.5905. Respironics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 12, 2021
Date Received
February 9, 2021
Clearance Type
Traditional
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