510(k) K053502
K053502 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 January 10, 2006. 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
- January 10, 2006
- Date Received
- December 16, 2005
- 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