Renaissance Medical, Inc.

Renaissance Medical, Inc. holds 4 FDA 510(k) medical device clearances, first cleared 1992, most recent 1994.

Top product codes for Renaissance Medical, Inc.

MGQ — Unknown4 devices

Recent clearances by Renaissance Medical, Inc.

K935203 — WOUND HYDROGEL AND/OR STERILE WOUND HYDROGELCode MGQ·1994-01-18
K932973 — ROYL-DERM WOUND HYDROGEL DRESSINGCode MGQ·1994-01-10
K933817 — ROYL-DERM WOUND HYDROGEL STERILE UNIT DOSECode MGQ·1994-01-10
K922815 — ROYL-DERM WOUND HYDROGELCode MGQ·1992-10-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.