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

IVENT 201

K Number: K053270 · Decision Jan 27, 2006
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
6
Review Days
65

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Basic Information

Device Name
IVENT 201
K Number
K053270
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Versamed Medical Systems, Inc.
Date Received
November 23, 2005
Decision Date
January 27, 2006
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.

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Other Clearances by Versamed Medical Systems, Inc.

K Number Device Name
K081845 IVENT101
K073694 IVENT 2001 MRI CONDITIONAL
K061627 MODIFICATION TO I VENT 201
K052554 MODIFICATION TO: IVENT 201 PORTABLE VENTILATOR
K042468 IVENT 201 PORTABLE VENTILATOR