Iriderm Div.
Iriderm Div. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1997.
Top product codes for Iriderm Div.
Recent clearances by Iriderm Div.
- K964074 — DIOLITE 532
- K960971 — OCULIGHT GL
- K960522 — DIOPEXY PROBE
- K915236 — IRIS G-PROBE
- K933211 — D'AMICO\PEYMAN FLUTED ENDOPROBE
- K922663 — IRIS OCULIGHT SL
- K913430 — IRIS OCULIGHT(R) SLX
- K912918 — IRIS OCULIGHT DIODE LASER ADDING SLIT LAMP ADAPTER
- K903288 — IRIS OCULIGHT SL DIODE LASER PHOTOCOAG/MODIFIED
- K894841 — IRIS OCULIGHT(TM) SL
Data sourced from openFDA. This site is unofficial and independent of the FDA.