Perimed, Inc.
Perimed, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1999.
Top product codes for Perimed, Inc.
Recent clearances by Perimed, Inc.
- K990960 — PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)
- K974285 — PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT
- K935495 — PF404/409/410/411/416/418 W/PF319:0/319:1/319:2
- K932068 — PERITEMP PF 4005 HEATER
- K922368 — PERIFLUX PF4001 LASER DOPPLER FLOWMETER
- K890828 — PERIFLUX PF3
Data sourced from openFDA. This site is unofficial and independent of the FDA.