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

MODEL 105 VENTILATOR, MODIFICATION

K Number: K922477 · Decision Aug 24, 1992
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
20
Review Days
89

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Basic Information

Device Name
MODEL 105 VENTILATOR, MODIFICATION
K Number
K922477
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Infrasonics Corp.
Date Received
May 27, 1992
Decision Date
August 24, 1992
Product Code
CBK
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
CBK Ventilator, Continuous, Facility Use

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K922654 VENTILATOR ADULT STAR MODIFICATION
K923704 INFANT STAR SERIES 500
K920954 AIR STAR
K911804 INFRASONICS VENTILATOR ADULT STAR, MODIFICATION
K913972 STAR SYNC, MODIFICATION
K905272 ADULT STAR, MODIFICATION
K896825 TRANSCUTANEOUS ELECTRONIC NERVE STIMULATOR
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