Meditec of America

Meditec of America holds 2 FDA 510(k) medical device clearances, first cleared 1984, most recent 1987.

Top product codes for Meditec of America

GEX — General, Plastic Surgery1 device
HQF — Ophthalmic1 device

Recent clearances by Meditec of America

K872578 — MDS-90 ARGON DYE LASER FOR DERMATOLOGYCode GEX·1987-10-01
K834610 — LASER LENS-VARIOUS MODELSCode HQF·1984-04-05

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