Atlas FDA

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

MQJ — Predicate Candidate Screening

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

33 daysmedian FDA review time
89 days90th percentile
23clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K142207TransferMan 4m MicromanipulatorEppendorf AG2015-01-231650
K120877MICROMANIPULATOR SETNarishige Co., Ltd.2012-06-20890
K113712IM-11 PNEUMATIC MICROINJECTORNarishige Co., Ltd.2012-03-15870
K011420MM-87 MOTOR-DRIVE MANIPULATORNarishige Co., Ltd.2001-06-12340
K010298MN-4 COARSE MANIPULATORNarishige Co., Ltd.2001-03-16440
K003303IM-5B MICROINJECTORNarishige Co., Ltd.2000-11-22330
K003300MO-202D THREE-AXIS HANGING JOYSTICK OIL HYDRAULIC MICROMANIPNarishige Co., Ltd.2000-11-22330
K003302IM-5A INJECTORNarishige Co., Ltd.2000-11-22330
K003304IM-6 MICROINJECTORNarishige Co., Ltd.2000-11-22330
K003142MICROMANIPULATORResearch Instruments , Ltd.2000-11-22430
K003298MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATORNarishige Co., Ltd.2000-11-21320
K002850MWO-202 3D HYDRAULIC COARSE/FINE MICROMANIPULATORNarishige Co., Ltd.2000-10-05220
K002653MMN-1 COARSE MANIPULATORNarishige Co., Ltd.2000-09-22280
K002659MMO-202ND THREE-AXIS HANGING JOYSTICK OIL HYDRAULIC MICROMANNarishige Co., Ltd.2000-09-22280
K002658MMO-202N THREE-AXIS JOYSTICK OIL HYDRAULIC MICROMANIPULATORNarishige Co., Ltd.2000-09-22280
K002291MOTOR-DRIVE MANIPULATOR MM-89Narishige Co., Ltd.2000-09-13480
K0022933D MOTOR-DRIVEN COARSE MANIPULATOR MM-188NENarishige Co., Ltd.2000-09-13480
K001912IM-9B MICROINJECTORSNarishige Co., Ltd.2000-07-07140
K001911IM-9A MICROINJECTORSNarishige Co., Ltd.2000-07-07140
K001910IM-9C MICROINJECTORSNarishige Co., Ltd.2000-07-07140
K0011303D MANUAL COARSE MANIPULATOR MN-188NENarishige Co., Ltd.2000-04-21110
K0011313D HDRAULIC FINE MICROMANIPULATOR MO-188NENarishige Co., Ltd.2000-04-21110
K993884GENX MICROTOOLS<Genx> Intl., Inc.2000-02-14900

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