Vitaid, Ltd.

7 FDA 510(k) medical device clearances.

Top product codes for Vitaid, Ltd.

BTR — Anesthesiology 3 devices
CBI — Anesthesiology 1 device
EZL — Gastroenterology, Urology 1 device
KOD — Gastroenterology, Urology 1 device
KPM — Gastroenterology, Urology 1 device

Recent clearances by Vitaid, Ltd.

K050803 — PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES BTR · 2005-06-30
K932647 — WIRE REINFORCED ENDOTRACHEAL TUBE BTR · 1993-11-02
K901738 — SELFCATH KOD · 1990-06-27
K894883 — PHYCON ALL SILICONE BALLOON CATHETER EZL · 1990-04-25
K894794 — AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP KPM · 1989-11-21
K894669 — LASER SHIELDING TUBE BTR · 1989-10-13
K894337 — UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM CBI · 1989-09-29

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