510(k) K931749
K931749 is an FDA 510(k) premarket notification submitted by Bivona Medical Technologies for the device "BIVONA(R) ICU ENDOTRACHEAL TUBE". The FDA issued a decision of Substantially Equivalent on Aug 10, 1993. The device falls under product code BTR (Tube, Tracheal (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5730. Bivona Medical Technologies has 49 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 10, 1993
- Date Received
- Apr 8, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Tube, Tracheal (W/Wo Connector)
- Device Class
- Class II
- Regulation Number
- 868.5730
- Review Panel
- AN
- Submission Type
- 510(k)