510(k) K913270
K913270 is an FDA 510(k) premarket notification submitted by Bivona Medical Technologies for the device "BIVONA FOME-CUF(R) PEDIATRIC TRACHEOSTOMY TUBE". The FDA issued a decision of Substantially Equivalent on August 9, 1991. The device falls under product code JOH (Tube Tracheostomy And Tube Cuff), a Class II device regulated under 21 CFR 868.5800. Bivona Medical Technologies has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 9, 1991
- Date Received
- July 23, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube Tracheostomy And Tube Cuff
- Device Class
- Class II
- Regulation Number
- 868.5800
- Review Panel
- AN
- Submission Type