Atlas FDA

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

Biomagnetic Technologies, Inc. — Predicate Candidate Screening

8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

117 daysmedian FDA review time
778 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K993708BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEGBiomagnetic Technologies, Inc.1999-12-03300
K962317MAGNES 2500 WH BIOMAGNETOMETERBiomagnetic Technologies, Inc.1997-05-073240
K941553MAGNES II BIOMAGNETOMETERBiomagnetic Technologies, Inc.1996-05-167780
K921821IBT MODEL SVIBiomagnetic Technologies, Inc.1992-11-022000
K913604SOMATOSENSORY STIMULUS SYSTEMBiomagnetic Technologies, Inc.1991-12-091170
K901215700 SERIES BIOMAGNETOMETERBiomagnetic Technologies, Inc.1990-06-251030
K854466BIOMAGNETIC TECHNOLOGIES NEUROMAGNEOMETERBiomagnetic Technologies, Inc.1986-02-04900
K790031GENERATOR, BIOTEC 876 PULSEBiomagnetic Technologies, Inc.1979-01-0200

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