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

Pilling Tracheostomy Tubes

K Number: K233713 · Decision Mar 22, 2024
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
39
Review Days
123

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Basic Information

Device Name
Pilling Tracheostomy Tubes
K Number
K233713
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teleflex Medical
Date Received
November 20, 2023
Decision Date
March 22, 2024
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)

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