510(k) K161314
K161314 is an FDA 510(k) premarket notification submitted by Flexicare Medical Limited. for the device "FLEXICARE FL-9000U RESPIRATORY HUMIDIFIER BASE". The FDA issued a decision of Substantially Equivalent on July 6, 2016. The device falls under product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5450. Flexicare Medical Limited. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 6, 2016
- Date Received
- May 11, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Humidifier, Respiratory Gas, (Direct Patient Interface)
- Device Class
- Class II
- Regulation Number
- 868.5450
- Review Panel
- AN
- Submission Type