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

Puritan Bennett 840 Series Ventilator System

K Number: K151252 · Decision Mar 29, 2016
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
3
Review Days
322

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Basic Information

Device Name
Puritan Bennett 840 Series Ventilator System
K Number
K151252
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien LP
Date Received
May 12, 2015
Decision Date
March 29, 2016
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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Other Clearances by Covidien LP

K Number Device Name
K091223 VALLEYLAB SUCTION COAGULATOR, MODEL E3305
K083350 TENS/NMES/FES STIMULATING ELECTRODE