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

EASYCARE TX, TX LINK

K Number: K092026 · Decision Oct 2, 2009
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
449
Applicant Total
90
Review Days
88

Basic Information

Device Name
EASYCARE TX, TX LINK
K Number
K092026
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RESMED LTD.
Date Received
July 6, 2009
Decision Date
October 2, 2009
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

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