Dio-Med Corp.
Dio-Med Corp. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1994.
Top product codes for Dio-Med Corp.
Recent clearances by Dio-Med Corp.
- K933525 — DIOMED 25 25W SURGICAL DIODE LASER
- K931776 — DIOMED 25 25W SURGICAL DIODE LASER
- K931212 — DIOMED 25 25W SURGICAL DIODE LASER
- K914519 — DIOMED 25 SURGICAL DIODE LASER, GYNECOLOGY APPLIC
- K914520 — DIOMED 25 SURGICAL DIODE LASER, UROLOGY APPLICAT
- K914521 — DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICAT
- K813267 — DISPOSABLE DIAPHRAGM DOMES
Data sourced from openFDA. This site is unofficial and independent of the FDA.