FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ENDOTRACHEAL TUBE

K Number: K080105 · Decision Feb 13, 2009
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
1
Review Days
396

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ENDOTRACHEAL TUBE
K Number
K080105
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Chilecom Medical Devices Co., Ltd.
Date Received
January 14, 2008
Decision Date
February 13, 2009
Product Code
BTR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTR Tube, Tracheal (W/Wo Connector)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BTR), ordered by most recent decision date.

View all