Renu Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K203847Reprocessed Tri Pulse Compression GarmentMay 7, 2021
K121145RENU MEDICAL REPROCESSED AIRCAST VENAFLOW CALF GARMENTS/ALL SIZES, RENU MEDICAL REPROCESSED AIRCAST June 12, 2012
K111773RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATENovember 16, 2011
K093658RENU MEDICAL VASOPRESS CALF , THIGH GARMENTS- ALL SIZESD, RENU MEDICAL VASOPRESS FOOT GARMENTSJanuary 14, 2010
K081927RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEOFebruary 6, 2009
K072194RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25November 29, 2007
K063661RENU REPROCESSED NELLCOR OXYSENSOR, MODELS D-20 AND I-20May 25, 2007
K051227RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1April 7, 2006
K031559RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVESNovember 12, 2003