Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Elder Pharmaceuticals, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K837106ELDER PSORALITE SERIES 2000 UVA IRRADIATION SYSTEMElder Pharmaceuticals, Inc.1983-03-22710
K837108ULTRAVIOLET ELDER PSORALITE SERIES 3000 UVAElder Pharmaceuticals, Inc.1983-03-22710
K837109UNKNOWNElder Pharmaceuticals, Inc.1983-03-22680
K837105ELDER PSORALITE, SERIES 43000Elder Pharmaceuticals, Inc.1983-03-07560

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