Vitaid, Ltd.

Vitaid, Ltd. holds 7 FDA 510(k) medical device clearances, first cleared 1989, most recent 2005.

Top product codes for Vitaid, Ltd.

Recent clearances by Vitaid, Ltd.

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

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