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

DEVILBISS INTELLIPAP/SLEEPCUBE BILEVEL S/ST

K Number: K091919 · Decision Sep 28, 2009
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
14
Review Days
90

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Basic Information

Device Name
DEVILBISS INTELLIPAP/SLEEPCUBE BILEVEL S/ST
K Number
K091919
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sunrise Medical
Date Received
June 30, 2009
Decision Date
September 28, 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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Other Clearances by Sunrise Medical

K Number Device Name
K123975 QUICKIE & ZIPPIE SERIES
K093070 DEVILBISS INTELLIPAP/ SLEEPCUBE BILEVEL ST, DV56 ST SERIES
K082209 DEVILBISS DV5M SMARTLINK SYSTEM
K081468 DEVILBISS PORTABLE OXYGEN CONCENTRATOR, 306 SERIES
K071397 DEVILBISS 5 LITER COMPACT OXYGEN CONCENTRATOR, MODEL 525 SERIES
K071689 DEVILBISS INTELLIPAP MODEL DV 5 SERIES
K060531 QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DELPHI CONTROLS
K053240 DEVILBISS OXYGEN CYLINDER FILLING SYSTEM, 535 SERIES
K043435 QUICKIE INTERCHANGE FWD W/LIFT POWER WHEELCHAIR
K043282 DEVILBISS AUTOADJUST, MODEL 9054 SERIES
Search all 14 clearances from Sunrise Medical →