Atlas FDA

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

Slt Labinstruments, Inc. — Predicate Candidate Screening

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

70 daysmedian FDA review time
190 days90th percentile
9clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K915689SLT SPECTRASlt Labinstruments, Inc.1992-04-221210
K915690SLT 340 ATTCSlt Labinstruments, Inc.1992-04-221210
K902776SPECTROPHOTOMETER (MICROASSAY PLATE READERS)Slt Labinstruments, Inc.1990-07-31360
K881797EASY WASHER II MICROPLATE WASHERSlt Labinstruments, Inc.1988-06-15490
K873678SPECTROPHOTOMETER (MICROASSAY PLATE READERS)Slt Labinstruments, Inc.1987-09-29150
K844894PHOTOMETER VARIOUS ONE FOR MICROTITERPLATESSlt Labinstruments, Inc.1985-06-251900
K844891SLT 225 WASHER/DISPENSER FOR MICRO TITERPLATESSlt Labinstruments, Inc.1985-02-25700
K844893SLT 223 DISPENSER FOR MICROTITERPLATESSlt Labinstruments, Inc.1985-02-25700
K844892SLT 220 WASHER FOR MICROITITERPLATESSlt Labinstruments, Inc.1985-02-25700

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