510(k) K122252
K122252 is an FDA 510(k) premarket notification submitted by Medical Developments International for the device "SPACE CHAMBER PLUS COMPACT SPACE CHAMBER PLUS". The FDA issued a decision of Substantially Equivalent on November 13, 2013. The device falls under product code NVP (Holding Chambers, Direct Patient Interface), a Class II device regulated under 21 CFR 868.5630.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 13, 2013
- Date Received
- July 27, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Holding Chambers, Direct Patient Interface
- Device Class
- Class II
- Regulation Number
- 868.5630
- Review Panel
- AN
- Submission Type
Holding chambers are devices that are used with nebulizers and metered dose inhalers and are comprised of a reservoir into which an aerosol medication is dispensed. A holding chamber uses a valved mouthpiece through which the patient inhales the dispensed medication. Holding chambers are intended to minimize delivery of large aerosolized particles