Dravon Medical, Inc.
Dravon Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1987.
Top product codes for Dravon Medical, Inc.
Recent clearances by Dravon Medical, Inc.
- K873455 — S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS
- K860770 — AM-100 I/A AMPAC
- K832739 — STEDIFLO INFUSION SET
- K831842 — DRAVON T CLAMP
- K812771 — PERITONEAL DIALYSIS DRAINAGE
- K812772 — PERITONEAL DIALYSIS CYCLER SET (8UNIT)
- K811851 — S-610 SHUNT ADAPTOR SET
- K800435 — HEMOSTATIC/TUBE OCCLUDING FORCEPS
- K782057 — CATHETER, RADIOPAQUE TENCKHOFF
- K782058 — CATHETER, BETA-CAP-PERITONEAL
- K781755 — DAP-PAK
- K780079 — CANNULA, ARTERY, RENAL
- K771097 — FORCEP, DISP., A CLAMP
- K760952 — TERASAKI LYMPHOCYTE TRANSPORT KIT
- K760994 — MONITOR LINE W/FILTER & NEEDLE
- K760995 — DECOLLATING TRAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.