Acuderm, Inc.
Acuderm, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1994.
Top product codes for Acuderm, Inc.
Recent clearances by Acuderm, Inc.
- K933516 — ACU-E PUNCH
- K933265 — ACU-DISPO-CE(TM)
- K933137 — ACU-SUTURE KIT
- K930043 — ACU-EVAC
- K933866 — ACU-HEMOSTATIC RING
- K915000 — ACU-GUARD
- K891334 — ACU-CURETTE
- K874024 — ACU-MICRO-NEEDLE
- K854877 — ACU-SYRINGE W/WO NEEDLES
- K832581 — DTM-DERMATOPHYTE TEST MEDIUM
- K832582 — MYCOSEL AGAR
- K832583 — SABOURAUD DEXTROSE AGAR
- K831635 — ACU-PUNCH
Data sourced from openFDA. This site is unofficial and independent of the FDA.