510(k) K013916

MELKER EMERGENCY CRICOTHYROTOMY CATHETER SET by Cook, Inc. — Product Code BWC

K013916 is an FDA 510(k) premarket notification submitted by Cook, Inc. for the device "MELKER EMERGENCY CRICOTHYROTOMY CATHETER SET". The FDA issued a decision of Substantially Equivalent on December 20, 2001. The device falls under product code BWC (Needle, Emergency Airway), a Class II device regulated under 21 CFR 868.5090. Cook, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 20, 2001
Date Received
November 27, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Emergency Airway
Device Class
Class II
Regulation Number
868.5090
Review Panel
AN
Submission Type