510(k) K830913
K830913 is an FDA 510(k) premarket notification submitted by Medlog GmbH Marketing Services for the device "MINITROP AEROSAL, PRODOMO AEROSAL AND". The FDA issued a decision of Substantially Equivalent on May 25, 1983. The device falls under product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5450. Medlog GmbH Marketing Services has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 25, 1983
- Date Received
- March 21, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Humidifier, Respiratory Gas, (Direct Patient Interface)
- Device Class
- Class II
- Regulation Number
- 868.5450
- Review Panel
- AN
- Submission Type