Renu Medical, Inc.
Renu Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2021.
Top product codes for Renu Medical, Inc.
Recent clearances by Renu Medical, Inc.
- K203847 — Reprocessed Tri Pulse Compression Garment
- K121145 — RENU MEDICAL REPROCESSED AIRCAST VENAFLOW CALF GARMENTS/ALL SIZES, RENU MEDICAL REPROCESSED AIRCAST VENAFLOW THIGH GARME
- K111773 — RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
- K093658 — RENU MEDICAL VASOPRESS CALF , THIGH GARMENTS- ALL SIZESD, RENU MEDICAL VASOPRESS FOOT GARMENTS
- K081927 — RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEO
- K072194 — RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25
- K063661 — RENU REPROCESSED NELLCOR OXYSENSOR, MODELS D-20 AND I-20
- K051227 — RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1
- K031559 — RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES
Data sourced from openFDA. This site is unofficial and independent of the FDA.