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

Pride Mobility Products Corp. — Predicate Candidate Screening

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

24 daysmedian FDA review time
157 days90th percentile
20clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K111739KIDS ROCK 3 CHAIRPride Mobility Products Corp.2011-08-12520
K091578LIFT CHAIR, MODEL T3Pride Mobility Products Corp.2009-12-021830
K092961JAZZY FRONTIEPride Mobility Products Corp.2009-10-23280
K092088VICTORY XL 130 FOUR WHEEL SCOOTER, MODEL SC713Pride Mobility Products Corp.2009-07-1670
K091113MAXIMA V, THREE WHEEL SCOOTER, MODEL SC900V MAXIMA V, FOUR WPride Mobility Products Corp.2009-05-11240
K090805V10, THREE WHEEL SCOOTER, MODEL SC610V, V10, THREE WHEEL SCOPride Mobility Products Corp.2009-04-0390
K090524GO GO ELITE TRAVELER V THREE WHEEL SCOOTER, MODEL SC40EVPride Mobility Products Corp.2009-03-19210
K072165VICTORY THREE WHEEL SCOOTER, MODEL: SC610Pride Mobility Products Corp.2007-08-17112
K071949VICTORY, 4 WHEEL SCOOTER / MODEL, # SC1740Pride Mobility Products Corp.2007-08-01191
K070950LIFT CHAIR, MODEL C5Pride Mobility Products Corp.2007-04-16120
K063389GO GO ELITE TRAVELLER PLUS 4 WHEEL SCOOTER, MODEL SC54Pride Mobility Products Corp.2006-11-17150
K062160GO GO MINI, MODEL SC30Pride Mobility Products Corp.2006-09-12460
K052353Z-CHAIRPride Mobility Products Corp.2005-09-09110
K042444LITESTREAM 500EPride Mobility Products Corp.2004-10-21420
K042612JAZZY 600Pride Mobility Products Corp.2004-10-06124
K041346SYNERGY ULTIMATEPride Mobility Products Corp.2004-09-081111
K011993QUANTUM BLASTPride Mobility Products Corp.2001-07-13173
K003058LASER 3 SPSC300Pride Mobility Products Corp.2001-03-081570
K003059LASER 4SPSC340Pride Mobility Products Corp.2001-03-011500
K001970JET 1 POWERED WHEELCHAIRPride Mobility Products Corp.2000-09-26901

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