Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Sunrise Medical · Predicate Candidate Screening

14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

90 daysmedian FDA review time
233 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K123975QUICKIE & ZIPPIE SERIESSunrise Medical2013-08-162335
K093070DEVILBISS INTELLIPAP/ SLEEPCUBE BILEVEL ST, DV56 ST SERIESSunrise Medical2010-01-261180
K091919DEVILBISS INTELLIPAP/SLEEPCUBE BILEVEL S/STSunrise Medical2009-09-28901
K082209DEVILBISS DV5M SMARTLINK SYSTEMSunrise Medical2008-10-28840
K081468DEVILBISS PORTABLE OXYGEN CONCENTRATOR, 306 SERIESSunrise Medical2008-08-25900
K071397DEVILBISS 5 LITER COMPACT OXYGEN CONCENTRATOR, MODEL 525 SERSunrise Medical2007-10-011333
K071689DEVILBISS INTELLIPAP MODEL DV 5 SERIESSunrise Medical2007-09-07792
K060531QUICKIE RHYTHM & GROOVE SERIES POWER WHEELCHAIRS W/QUICKIE DSunrise Medical2006-03-17174
K053240DEVILBISS OXYGEN CYLINDER FILLING SYSTEM, 535 SERIESSunrise Medical2006-02-03771
K043282DEVILBISS AUTOADJUST, MODEL 9054 SERIESSunrise Medical2005-02-11770
K043435QUICKIE INTERCHANGE FWD W/LIFT POWER WHEELCHAIRSunrise Medical2005-02-11600
K042455DEVILBISS NASAL CPAP MASK, 9354 SERIESSunrise Medical2005-01-141260
K032056BILEVEL CPAP, MODEL 9055 SERIESSunrise Medical2004-02-202330
K020932DEVILBISS PULMO-AIDE COMPACT COMPRESSORSunrise Medical2002-06-28980

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda