510(k) K924195

TRACHEOSTOMY CARE SET W/FORCEPS & GAUZE TRACH DRES by American Healthcare Corp. — Product Code BTO

K924195 is an FDA 510(k) premarket notification submitted by American Healthcare Corp. for the device "TRACHEOSTOMY CARE SET W/FORCEPS & GAUZE TRACH DRES". The FDA issued a decision of Substantially Equivalent on January 6, 1993. The device falls under product code BTO (Tube, Tracheostomy (W/Wo Connector)), a Class II device regulated under 21 CFR 868.5800. American Healthcare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 6, 1993
Date Received
August 20, 1992
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