Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

JMO — Predicate Candidate Screening

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

47 daysmedian FDA review time
106 days90th percentile
46clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K113438ACE DIRECT TOTALIRON-BINDING CAPACITY (TIBC) REAGENT, ACE SEAlfa Wassermann Diagnostic Technologies, Inc.2012-06-011930
K061464VITROS CHEMISTRY PRODUCTS TIBC KIT, MODEL 886 7541; CALIBRATOrtho-Clinical Diagnostics, Inc.2006-06-15210
K052867VITROS CHEMISTRY PRODUCTS DTIBC REAGENTOrtho-Clinical Diagnostics, Inc.2005-12-23730
K041793OLYMPUS UNSATURATED IRON BINDING CAPCITY REAGENT, OSR6124/0SOlympus America, Inc.2004-07-16141
K013102WIENER LAB. FER-COLOR TRANSFERRINA, MODEL AUX. REAGENTS FOR Wiener Laboratories Saic2001-11-13570
K012340BAYER ADVIA SYSTEM; UNSATURATED IRON BINDING CAPACITY (UIBC)Bayer Corp.2001-10-01690
K000781DIRECT TIBC KITReference Diagnostics, Inc.2000-05-02530
K994115TOTAL IRON BINDING CAPACITY (IBCT) FLEX REAGENT CARTRIDGEDade Behring, Inc.2000-01-28532
K991666TIBC, PRODUCT NO'S 123-0, 123-02, FE109-01, FE109-02A.P. Total Care, Inc.1999-06-30470
K991244TOTAL IRON, MODELS FE 109-01, FE 109-02A.P. Total Care, Inc.1999-05-25430
K990216MAGNETIC TIBC KITReference Diagnostics, Inc.1999-02-16250
K982041UIBCAbbott Laboratories1998-07-30500
K981654TIBCAbbott Laboratories1998-07-22720
K981279TIBCAbbott Laboratories1998-05-20420
K974604RANDOX IRONRandox Laboratories, Ltd.1998-01-06270
K961587IRON (TOTAL) ASSAY CATALOGUE NO. 102-10, 102-25Diagnostic Chemicals , Ltd.1996-08-271251
K963116UNSATURATED IRON BINDING CAPACITY (UIBC) ASSAYDiagnostic Chemicals , Ltd.1996-08-2080
K960485SYNCHRON SYSTEMS IRON (FE)/TOTAL IRON BINDING CAPACITY REAGEBeckman Instruments, Inc.1996-05-10980
K955139OLYMPUS UNSATURATED IRON BINDING CAPACITY REAGENTOlympus America, Inc.1996-02-12910
K946354DMA UNSATURATED IRON BINDING CAPACITY PROCEDUREData Medical Associates, Inc.1995-05-081290
K932517IRON/UIBC REAGENTSigma Diagnostics, Inc.1993-11-091680
K933329KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENKing Diagnostics, Inc.1993-10-221060
K931493KODAK EKTACHEM TOTAL IRON-BINDING CAPACITY KITEastman Kodak Company1993-05-26620
K923569PARAMAX TOTAL IRON BINDING CAPACITY PRETREATMENTBaxter Diagnostics, Inc.1992-08-26400
K922784SYNERMED UIBC REAGENT KITSynermed, Inc.1992-07-21420
K912716J&S IRON REAGENTSJ.S. Medical Assoc.1991-09-25990
K912717J&S UIBC REAGENTSJ.S. Medical Assoc.1991-09-25990
K913922ABBOTT QUICKSTART TIBC PRETREATMENT KIT, 5A29-01Em Diagnostic Systems, Inc.1991-09-19160
K912795BIOTROL UIBC REAGENTBiotrol, USA, Inc.1991-08-12480
K904116IRON 5 X CONC REAGENTTrace Scientific , Ltd.1990-09-27210
K901960IRON REAGENTS PRODUCT CODES 7725 AND 7726American Research Products Co.1990-05-31300
K893662J&S IRON SATURATING REAGENTSJ.S. Medical Assoc.1989-07-20660
K883104CHEM 1 UIBC (IRON BINDING CAPACITY TEST)Technicon Instruments Corp.1988-10-25920
K881761UNSATURATED IRON BINDING CAPACITYData Medical Associates, Inc.1988-07-08740
K880546TOTAL IRON BINDING CAPACITY (TIBC)Boehringer Mannheim Corp.1988-03-24440
K874055IRON REAGENTTrace Scientific , Ltd.1987-10-28230
K871414EMDS TIBC PRETREATMENT SET ITEM NO. 67612/93Em Diagnostic Systems, Inc.1987-04-23150
K863426AMRESCO FLOW PAC TOTAL IRON REAGENT SET #1241American Research Products Co.1986-09-16120
K851930TDX REA IRON/TIBCAbbott Laboratories1985-05-24220
K851395SANDARE IRON-BINDING CAPACITY PROCEDURESandare Chemical Co., Inc.1985-05-07280
K850128SYSTE MATE TIBC HEM NO. 67225Em Diagnostic Systems, Inc.1985-02-01180
K832759TOTAL IRON-BINDING CAPACITY ACCESORYSeragen Diagnostics, Inc.1983-10-14560
K831202SERUM UIBC-PTF-600 METHODAmerican Monitor Corp.1983-05-25420
K780094IRON BINDING CAPACITY CHEMISTRYHarleco1978-02-13260
K771927IRON SET, ITEM NO. 65008Harleco1977-11-14310
K770748TEST, FERROZINE IRON & IRON BINDINGHycel, Inc.1977-06-01400

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