FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH

K Number: K100480 · Decision Jun 11, 2010
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
2
Review Days
113

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Basic Information

Device Name
ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH
K Number
K100480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vitaltec Corporation
Date Received
February 18, 2010
Decision Date
June 11, 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 Vitaltec Corporation

K Number Device Name
K242921 5300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm; 5310600-5311000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, Fenestrated, sizes 6.0-10.0mm; 5400600-5401000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, sizes 6.0-10.0mm; 5410500-5411000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, Fenestrated, sizes 6.0-10.0mm