510(k) K781729
K781729 is an FDA 510(k) premarket notification submitted by Tracoe Medical GmbH for the device "TRACHEOTOMY TUBES". The FDA issued a decision of Substantially Equivalent on October 24, 1978. The device falls under product code BTO (Tube, Tracheostomy (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5800. Tracoe Medical GmbH has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 24, 1978
- Date Received
- October 10, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tube, Tracheostomy (W/Wo Connector)
- Device Class
- Class II
- Regulation Number
- 868.5800
- Review Panel
- AN
- Submission Type