Atlas FDA

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

Evergreen Technologies, Inc. — Predicate Candidate Screening

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

115 daysmedian FDA review time
173 days90th percentile
7clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K942861MEDVISION ENVIROMENT/MEDVISION 2.0Evergreen Technologies, Inc.1994-12-071730
K942860VISIONLINK DICOM MODULEEvergreen Technologies, Inc.1994-09-16910
K935103VISIONLINK ACR-NEMA CONVERSION UTILITIESEvergreen Technologies, Inc.1994-02-091070
K933372VISIONLINK INTERFILE CONVERSION SOFTWAREEvergreen Technologies, Inc.1993-11-011150
K933209VISIONTOOLEvergreen Technologies, Inc.1993-09-29900
K924178MEDVISION(TM) IMAGING SOFTWAREEvergreen Technologies, Inc.1993-02-021670
K921484MEDVISIONEvergreen Technologies, Inc.1992-08-071300

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