Atlas FDA

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

KPT — Predicate Candidate Screening

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

76 daysmedian FDA review time
209 days90th percentile
32clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K192199CRC PC Smart Chamber K1Capintec, Inc.2019-09-12300
K162394CRC-77tHRCapintec, Inc.2017-03-081940
K142325Veenstra Instruments VDC-506 Dose CalibratorComecer Netherlands B.V.2014-09-18290
K141413CRC PC WITH SMART CHAMBERCapintec, Inc.2014-06-27290
K101452CAPINTEC CRC 55T SERIES DOSE CALIBRATORS, MODELS CRC 55TR, CCapintec, Inc.2010-08-09760
K090296ATOMLAB 400 AND ATOMLAB 500 DOSE CALIBRATORS, MODELS 086-330Biodex Medical Systems, Inc.2009-02-19130
K071396CRC 25 SERIES (CRC 25R, CRC 25PET, CRC 25W) DOSE CALIBRATORSCapintec, Inc.2007-06-28381
K042746PET-DOSEComecer S.R.L.2004-11-22490
K030066CAL/RAD MARK VI/VDC-505 DOSE CALIBRATOR, MODEL 34-165Nuclear Associates2003-08-292340
K011493MENTOR ISOLOADER AUTOMATIC NEEDLE LOADING SYSTEM AND PHYSICSMentor Corp.2002-10-015040
K020150CRC-15BTCapintec, Inc.2002-08-021980
K013689RE-ENTRANT CHAMBERSun Nuclear Corp.2002-07-022380
K013548STANDARD IMAGING IVB 1000 WELL CHAMBERStandard Imaging, Inc.2001-11-09160
K010417CAL/RAD MARK IV-DOSE CALIBRATOR 34-162 VEENSTRA MODEL # VDC-Nuclear Assoc., Div. Inovision LP2001-04-26730
K002833MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBERStandard Imaging, Inc.2000-09-28160
K943072BETA C COUNTERCapintec Instruments, Inc.1994-09-29930
K935539CAPINTEC CRC 35RCapintec Instruments, Inc.1994-02-18940
K931657NUCLEAR ASSOCIATES MODEL 34-070 BRACHYTHERAPY CAL.Victoreen, Inc.1993-07-271130
K905796DOSE CALIBRATORCapintec Instruments, Inc.1991-03-18810
K884312ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270Atomic Products Corp.1989-02-161260
K880272CAL/RAD UPGRADE MODEL 1030Sun Nuclear Corp.1988-02-29390
K850838CLINICOMP RDMS RADIONUCLIDE DISPENSING MGMT. SOFTWClinicomp, Inc.1985-09-262090
K850815RADIOISOTOPE CALIBRATOR MODEL 34-062Victoreen, Inc.1985-08-211740
K842540CLINICOMP R.C.I.Clinicomp, Inc.1984-08-08370
K842570LUDLUM 88 DOSE CALIBRATORLudlum Measurements, Inc.1984-08-07350
K841785RADCAL MODEL 4046 RADIONUCLIDE CALIBRRadcal Corp.1984-07-16770
K841786RADCAL MODEL 4051 RADIONUCLIDE CALIBRARadcal Corp.1984-07-16770
K841787RADCAL MODEL 4050 RADIONUCLIDE CALIBRadcal Corp.1984-07-16770
K813379RADIONUCLIDE DOSE CALIBRATORMedi Nuclear Corp., Inc.1982-01-22520
K813065B.D.A.S.General Electric Co.1981-12-08390
K811320CAL-3 CALIBRATED RADIOACTIVITY ASSAYERDosimeter Corp.1981-06-02210
K770515DISPENSER, TECHNETIUM, CLINTICHEMUnion Carbide Corp.1977-04-05190

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