Atlas FDA

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

IME · Predicate Candidate Screening

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

30 daysmedian FDA review time
170 days90th percentile
27clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K923627COLD PACKFriendmed Products1993-04-142670
K915876HOTPADTen Comfort Corp.1993-02-124210
K921446HOT OR COLD PACK (THERMIPAQ)Thermionics Corp.1992-07-131080
K905207MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESSMicro Surgical Instruments Corp.1991-01-22630
K882413SUBOCCIPITAL ICE PILLOWFerguson Medical1988-11-301700
K863654RE-HEATER, HOT PACKK & L Ent.1986-10-23350
K832193NICE PACKUniversal Medical Instrument Corp.1983-08-31540
K831899ENSWELLDr. Micheal A. Sabia1983-07-07230
K830981MICROPAK MOIST HEAT PADMicropak Manufacturers, Inc.1983-06-03660
K830416ICY COLD ICE CAPLadora Ent.1983-03-10300
K823649THERMOELASTOMER HOT/COLD COMPRESS BK7186Fred Sammons, Inc.1983-01-21460
K823650THERMOELASTOMER HOT/COLD COMPRESS-7187-Fred Sammons, Inc.1983-01-21460
K823814HOT/COLD PACK HOLDERSDanek Medical, Inc.1983-01-14280
K822783FLEX ICE FREEZE PACKIgloo Corp.1982-10-06220
K821636ATTACH-A-PAKFred Sammons, Inc.1982-06-1180
K820901COLD ROLLNorth Bank Labs, Inc.1982-04-15150
K820068COLD-HOT PACKHospital Marketing Services Co., Inc.1982-01-28160
K810451REUSEABLE HOT & COLD PACKSFred Sammons, Inc.1981-03-04130
K810402ACE COLD BANDAGEBd Becton Dickinson Vacutainer Systems Preanalytic1981-03-04140
K803299COLD/HOT PACKW.G. Whitney Corp.1981-01-15160
K801776COLD PACK #589Sunbeam Corp.1980-08-07100
K801365KOLD WRAPRomaine, Inc.1980-08-07580
K800917TRU-COLD THERAPY PAKTru-Eze Mfg. Co., Inc.1980-05-02100
K792182ICE CONTAINER I.C.E.Delta Medical Industries1979-11-15170
K791684WARM-EE HEAT PACKU.S. Export Marketing Group, Inc.1979-10-30630
K790009ICE PACK, REUSABLE FLEXIBLEAckrad Laboratories1979-01-22200
K771002ICE BANDNorcliff Thayer, Inc.1977-08-30890

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