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

FLIGHT 60 VENTILATOR

K Number: K130171 · Decision Apr 8, 2014
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
5
Review Days
439

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FLIGHT 60 VENTILATOR
K Number
K130171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Flight Medical Innovations , Ltd.
Date Received
January 24, 2013
Decision Date
April 8, 2014
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.

View all

Other Clearances by Flight Medical Innovations , Ltd.

K Number Device Name
K223120 Ventoux VC2; Ventoux VC3
K143035 Flight 60 Ventilator
K120726 FLIGHT 60 VENTILATOR
K111683 FLIGHT 60 VENTILATOR