510(k) K983000

CRICOTHYROTOMY TUBE by Polamedco, Inc. — Product Code BTO

K983000 is an FDA 510(k) premarket notification submitted by Polamedco, Inc. for the device "CRICOTHYROTOMY TUBE". The FDA issued a decision of Substantially Equivalent on October 27, 1999. The device falls under product code BTO (Tube, Tracheostomy (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5800. Polamedco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1999
Date Received
August 27, 1998
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