Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Grace River Ent., Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K902803 A PHYSIOTHERAPY APPARATUSILY1991-02-06 View
510(k) K891277 PATIENT EXAMINATION GLOVES (LATEX)LYY1990-01-11 View
↑