Atlas FDA

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

FPP — Predicate Candidate Screening

39 FDA 510(k) clearances under this product code; the 50 most recent screened below.

63 daysmedian FDA review time
225 days90th percentile
39clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K030283BABY PODPrism Enterprises, Inc.2003-04-22850
K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.1994-07-19630
K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.1994-03-10660
K940245EVACU-SLEDEvacu Technologies, Inc.1994-02-28400
K924275RESTRAINING STRETCHERDms1993-07-273360
K922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, Inc.1993-07-133970
K924669FERNO-WASHINGTON BASKET STRETCHER, MODEL 71-WFerno1993-04-292250
K920805LIFE LITE EMERGENCY STRETCHERDesign Principles, Inc.1992-05-22910
K915874BASKET LITTER CARRIERBradco Med , Ltd.1992-05-131560
K914140GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEEDBissell Medical Products, Inc.1992-03-311970
K913520EVACU SLEDNexus Health Care Products , Ltd.1991-12-041190
K911765HAND CARRIED STRETCHERL.E. Phillips Career Development Center, Inc.1991-06-14560
K904237RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEMInnovative Medical Technologies, Inc.1991-05-092340
K910709WEEVAC TC HAND CARRIED RESCUE STRETCHERW. Murphy Ent., Inc.1991-04-01400
K905381MANHANDLERLifeport, Inc.1991-03-131040
K904261LITTER, NONRIDGID, POLELESS, NYLON STRETCHERDow Cover Co., Inc.1990-10-12280
K904494HAND-CARRIED STRETCHERSMinto Research & Development, Inc.1990-10-12100
K904511HAND-CARRIED STRETCHERS/BREAK AWAY FLATMinto Research & Development, Inc.1990-10-12100
K902474WEEVAC 1 PORTABLE RESCUE STRETCHERW. Murphy Ent., Inc.1990-07-24490
K901760LITTER, FOLDING RIGID POLE, DECONTAMINABLEDept. of the Army1990-07-10830
K902521WEEVAC 6 INFANT EVACUATION STRETCHERW. Murphy Ent., Inc.1990-06-22150
K900670HARE EMERGENCY STRETCHERDyna Corp.1990-04-23690
K900671HARE EMERGENCY STRETCHER WITH WHEELSDyna Corp.1990-04-23690
K896179SKED FLOTATION SYSTEMSkedco, Inc.1990-01-11780
K896177SKED STRETCHERSkedco, Inc.1990-01-11780
K896261THE SMITHCOTRam Marketing, Inc.1989-12-22530
K892892NET STRETCHER PAD (TM)North East Technology1989-11-212150
K871629FOLDING LITTER SUPPORT, NSN6530-00-660-0034Junkin Safety Appliance Co., Inc.1987-05-0690
K870327BACK REST, LITTER, NONADJUSTABLEMilitary Engineering, Inc.1987-02-10130
K863686BACK REST, LITTER, NON-ADJUSTABLEBrenner Metal Prod Corp.1987-01-201230
K863511IMMOBILIZING VACUUM MATRESS (IVM)Omnium Services Partners, Inc.1986-09-25160
K851660DONWAY LIFTING FRAMEAustralian Biomedical Corporation , Ltd.1985-08-071060
K840034VACUUM STRETCHER IMMOBILIZERMedicon, Inc.1984-02-27530
K831731INFANT EVALUATION CARRIERE.M. Adams1983-07-18480
K811547MATELAS COQUILLE LATTREDE TASSIGNYFirn-France1981-06-18170
K810868ARALUEN HEAD SHIELDAraluen, Inc.1981-05-13430
K810922ARALUEN SKY GRAB BRIDLEAraluen, Inc.1981-04-29230
K792566THE ARALUEN CARRIERAraluen, Inc.1979-12-2070
K770911MEDISHIELD JORDON LIFTING FRAMEFraser Sweatman, Inc.1977-06-27390

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