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.

Perimed, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K990960 PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)LKD1999-09-23 View
510(k) K974285 PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNITDPW1998-05-28 View
510(k) K935495 PF404/409/410/411/416/418 W/PF319:0/319:1/319:2GEX1994-04-18 View
510(k) K932068 PERITEMP PF 4005 HEATERDPW1993-12-07 View
510(k) K922368 PERIFLUX PF4001 LASER DOPPLER FLOWMETERDPW1993-02-03 View
510(k) K890828 PERIFLUX PF3DPW1989-06-20 View
↑