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.

Gespac, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K892522 SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIEDGKB1989-05-24 View
510(k) K890503 SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATEGKB1989-02-10 View
↑