Distronic Sterile Products, Inc.
Distronic Sterile Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 1996.
Top product codes for Distronic Sterile Products, Inc.
Recent clearances by Distronic Sterile Products, Inc.
- K955709 — WINGED & SUBCUTANEOUS INFUSION SETS
- K955732 — VENTED SOLUTION SET
- K954983 — EXTENSION SET WITH CHECK VALVE
- K954984 — MINIBORE STOPCOCK SET
- K952664 — SOLUTION ADMINISTRATION SET
- K950597 — CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE
- K952663 — 60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON GILYRT, INJ. SITE, CLAMP
- K945184 — INTRAVASCULAR ADMINISTRATION SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.