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Perimed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K152930PeriFlux6000May 5, 2016
K131253PERIFLUX 6000October 22, 2013
K120884PERICAM PSIJuly 3, 2012
K011899PF 5050 PRESSURE UNIT, MODEL PF 5050November 6, 2001
K990960PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)September 23, 1999
K974285PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNMay 28, 1998
K935495PF404/409/410/411/416/418 W/PF319:0/319:1/319:2April 18, 1994
K932068PERITEMP PF 4005 HEATERDecember 7, 1993
K922368PERIFLUX PF4001 LASER DOPPLER FLOWMETERFebruary 3, 1993
K890828PERIFLUX PF3June 20, 1989