510(k) K781729

TRACHEOTOMY TUBES by Tracoe Medical GmbH — Product Code BTO

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