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

TRACHEOSTOMY T-TUBE

K Number: K930114 · Decision Mar 19, 1993
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
16
Review Days
67

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Basic Information

Device Name
TRACHEOSTOMY T-TUBE
K Number
K930114
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Invotec International, Inc.
Date Received
January 11, 1993
Decision Date
March 19, 1993
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)

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