510(k) K101803
K101803 is an FDA 510(k) premarket notification submitted by Newport Medical Instruments, Inc. for the device "NEWPORT E360 VENTILATOR". The FDA issued a decision of Substantially Equivalent on September 8, 2010. The device falls under product code CBK (Ventilator, Continuous, Facility Use), a Class II device regulated under 21 CFR 868.5895. Newport Medical Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 2010
- Date Received
- June 28, 2010
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ventilator, Continuous, Facility Use
- Device Class
- Class II
- Regulation Number
- 868.5895
- Review Panel
- AN
- Submission Type