Atlas FDA

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

KCY · Predicate Candidate Screening

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

68 daysmedian FDA review time
233 days90th percentile
34clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K202919ATS 5000 Automatic Tourniquet InstrumentMcewen and Associates Consulting , Ltd.2021-05-202331
K162365T-CuffTerumobct, Inc.2017-02-161770
K123553ZIMMER A.T.S. 4000TS AUTOMATIC TOURNIQUET SYSTEMZimmer, Inc.2013-08-092630
K112874EZ VEIN INFLATABLE TOURNIQUETDominion Medical Devices, LLC2011-10-17170
K071140MRI COMPATIBLE THIGH TOURNIQUET, MODEL C070002Top Spins, Inc.2007-06-07440
K050411ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEMZimmer, Inc.2005-09-021971
K012632TOURNIQUET CUFF; PNEUMATIC TOURNIQUETMedical Instruments Technology, Inc.2001-10-26740
K955552EXPRESSAIRE TORUNIQUET SYSTEMSmith & Nephew Richards, Inc.1996-01-05310
K954201BUONAFEDE PNEUMATIC SLEEVEPromedic, Inc.1995-11-09640
K954103TOURNI-COMPScandinavian Medical JW AB1995-11-01620
K953953DEROYAL INDUSTRIES, INC. PNEUMATIC TOURNIQUET CUFFDeroyal Industries, Inc.1995-09-29380
K952038CLEAN-CUFFInstrumed, Inc.1995-07-11711
K940615ACCUTESTInstrumed, Inc.1995-05-194590
K945167DJ MEDICAL PNEUMATIC TOURNIQUETDj Medical, Inc.1995-02-131440
K942303TECNADYNE T-CUFFTechnadyne Scientific, Inc.1994-07-20680
K933994ARTHREX TOURNIQUET FOR LEG HOLDERArthrex, Inc.1994-03-232180
K925033STILLE AUTOMATIC TOURNIQUETFerguson Medical1993-02-011190
K924273ACCUFLATEInstrumed, Inc.1993-01-121413
K910449PRESTITCHCrantec Co.1992-05-294860
K910512ACCUFLATEInstrumed, Inc.1991-02-19140
K900104TCPM II TOURNIQUET CUFF PRESSURE MONITORElectromedics, Inc.1990-03-15650
K890014DISPOSABLE COLOR-CUFFSInstrumed, Inc.1989-01-24210
K8800203 IN 1 AUTOMATIC TOURNIQUETSystematics Mfg. & Tool Co., Inc.1988-03-17720
K871982TOURNIQUET PRESSURE REGULATORAvec Scientific Design Corp.1987-06-09180
K870784A.T.S. 1500 TOURNIQUETAspen Laboratories, Inc.1987-03-18200
K860463SINGLE AND DUAL TOURNIQUET CUFFAspen Laboratories, Inc.1986-02-25190
K860095DIGIKIT NONPNEUMATIC TOURNIQUETOrthofab, Inc.1986-01-24140
K853802ATS 500 TOURNIQUETAspen Laboratories, Inc.1985-10-07260
K842963RHYS-DAVIES EXSANGUINATORWoodville Polymer Engineering, Ltd.1984-08-17210
K841558BANANA CUFFAspen Laboratories, Inc.1984-07-16910
K840206PRESSURE SENTRY TOURNIQUETRichards Medical Co., Inc.1984-04-25970
K813231TOURNIQUETAspen Laboratories, Inc.1981-12-14270
K791759TEST PRESSURE GAUGE #6675-32Depuy, Inc.1979-10-04290
K780988DEVIN-NESTOR PNEUMATIC TOURNIQUETNestor Engineering Associates, Inc.1978-10-031110

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