Atlas FDA

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

GDM — Predicate Candidate Screening

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

56 daysmedian FDA review time
174 days90th percentile
48clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K071732MARROWMINERStemcor Systems, Inc.2007-09-24900
K971114BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.1997-06-03690
K953082ILIAC CREST BONE MARROW ASPIRATION NEEDLEBaxter Healthcare Corp1995-09-22810
K953064BIOACCESS MARROW HARVEST SYSTEMBioaccess, Inc.1995-08-07380
K936207ENDO-NEEDLE INSTRUMENTGerard Medical, Inc.1994-06-161690
K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.1993-07-061740
K923872BONE MARROW BIOPSY SYSTEMThe Straumann Co.1992-12-151340
K915572BECTON DICKINSON MODIFIED MENGHINI NEEDLEBd Becton Dickinson Vacutainer Systems Preanalytic1992-02-03530
K904667NA NEEDLESOlympus Corp.1990-12-12580
K903747ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-UDowns Surgical , Ltd.1990-10-31760
K903750ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-EDowns Surgical , Ltd.1990-10-31760
K903749ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-UDowns Surgical , Ltd.1990-10-31760
K903748ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-VDowns Surgical , Ltd.1990-10-31760
K902177MANAN BONE BIOPSY NEEDLEManan Medical Products, Inc.1990-09-051130
K901995PLEURA BIOPSY DEVICEMill-Rose Laboratory1990-07-10690
K895752DIAMOND BLADE SURGICAL KNIVESMagnum Diamond, Inc.1989-10-17210
K895551ROCKET BONE MARROW NEEDLEA & A Medical, Inc.1989-10-06230
K895594SINGLE LUMEN O'NEIL ASPIRATION & IRRIGATION NEEDLEGo Medical Industries Pty. , Ltd.1989-10-06210
K890722ADG BONE BIOPSY SYSTEMAmerican Design Group, Inc.1989-09-212200
K891537CORE BIOPSY NEEDLE, CATALOG CODE #54006Dlp, Inc.1989-04-18320
K885283ASPIRATING AND IRRIGATING CYSTS NEEDLESGo Medical Industries Pty. , Ltd.1989-03-22920
K881783KLEIN HANDLEE.L. Medico Intl., Inc.1988-12-022200
K881784KLEIN NEEDLEE.L. Medico Intl., Inc.1988-12-022190
K883876WILLIAMS-FRITTS PLEURAL BIOPSY NEEDLEE.G. Dick & Assoc.1988-10-07240
K881624PLEURAL BIOPSY PUNCH NEEDLEE.G. Dick & Assoc.1988-08-111210
K882240STORZ UNIV IRRIGAT/ASPIRA & PHACOEMULSIFCATION PACStorz Instrument Co.1988-07-29630
K882601E-Z-EM(R) LUFKIN BIOPSY NEEDLESE-Z-Em, Inc.1988-07-25310
K882073SPINAL NEEDLEKarlin Technology, Inc.1988-07-18620
K881730BREAST LOCALIZATION NEEDLESHart Enterprises, Inc.1988-05-13210
K880812SPINAL NEEDLET. Korossurgical Instruments Corp.1988-03-11140
K874928WHOLEY (TM) BIOPSY DEVICEMedrad, Inc.1987-12-30280
K873848RETROBULBAR NEEDLEHealthtek, Inc.1987-10-23310
K870523HAWKINS BREAST LOCALIZATION NEEDLEN-S Medical Products1987-03-09311
K864193GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUNGaw, Inc.1986-11-17210
K862805ANGIOMED VAC-U-CUT BIOPSY NEEDLEAngiomed U.S., Inc.1986-09-29690
K862749LS9000 SUCTION BIOPSY NEEDLEEngineering, Inc.1986-09-15560
K862481CIVCO/KEMPF ASPIRATION/BIOPSY/DIALYSIS NEEDLECIVCO Medical Instruments Co., Inc.1986-07-23230
K854420MEADOX SURGIMED A/S THREE PIECE SCREW BIOPSY NEEDLMeadox Surgimed, Inc.1985-11-22180
K843830J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPIPopper & Sons, Inc.1984-10-26250
K843690ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLEPopper & Sons, Inc.1984-10-25360
K833720TRANSTHORACIC/TRANSABDOMINAL-TRAYApplied Medical Devices, Inc.1984-05-302190
K841299BIERMAN BIOPSY NEEDLEPopper & Sons, Inc.1984-05-02330
K830235FRANZEN NEEDLE GUIDEPrecision Dynamics Corp.1983-02-23290
K820339ISLAM BONE MARROW BIOPSY NEEDLEDowns Surgical , Ltd.1982-02-23150
K800406FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLEA.D.T. Lab Industries1980-03-12150
K791643BONE MARROW NEEDLEJohannah Medical Services, Inc.1979-09-12200
K772293BONE MARROW BIOPSY DEVICERadiation Development Co., Inc.1978-01-03220
K771574LEE ASPIRATION NEEDLERadiation Development Co., Inc.1977-12-061130

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