510(k) K903730

D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES by Concord/Portex — Product Code BTO

K903730 is an FDA 510(k) premarket notification submitted by Concord/Portex for the device "D.I.C. TRACHEOSTOMY TUBES & LARYNGECTOMY TUBES". The FDA issued a decision of Substantially Equivalent on September 25, 1990. The device falls under product code BTO (Tube, Tracheostomy (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5800. Concord/Portex has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 1990
Date Received
August 16, 1990
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