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

VENNER PNEUX P.Y. (TM) TRACHEOSTOMY TUBE

K Number: K100950 · Decision Jul 13, 2010
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
6
Review Days
98

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Basic Information

Device Name
VENNER PNEUX P.Y. (TM) TRACHEOSTOMY TUBE
K Number
K100950
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Venner Medical (Singapore) Pte, Ltd.
Date Received
April 6, 2010
Decision Date
July 13, 2010
Product Code
BTO
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
BTO Tube, Tracheostomy (W/Wo Connector)

Similar 510(k) Clearances

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

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Other Clearances by Venner Medical (Singapore) Pte, Ltd.

K Number Device Name
K192511 Venner PneuX™ TT (Tracheostomy Tube) Size 7.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 8.0 mm, Venner PneuX™ TT (Tracheostomy Tube) Size 9.0 mm
K192120 Venner PneuX™ ETT (Endotracheal Tube) 6 mm, Venner PneuX™ ETT (Endotracheal Tube) 7 mm, Venner PneuX™ ETT (Endotracheal Tube) 8 mm, Venner PneuX™ ETT (Endotracheal Tube) 9 mm
K191602 APA Oxy Blade
K110631 VENNER TRACHEAL SEAL MONITOR
K093135 VENNER PNEUX P.Y. (TM) TRACHEOSTOMY TUBE AND ENDO TRACHEAL TUBE