The Kendall Company Div. of Tyco Healthcare Group

The Kendall Company Div. of Tyco Healthcare Group holds 4 FDA 510(k) medical device clearances, first cleared 1983, most recent 2003.

Top product codes for The Kendall Company Div. of Tyco Healthcare Group

Recent clearances by The Kendall Company Div. of Tyco Healthcare Group

K024010 — DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETERCode EZL·2003-06-11
K831081 — EZEE FILTER/SEPARATORCode JKA·1983-05-16
K831082 — CONNECTING TUBINGCode BYX·1983-05-09
K831079 — LIQUIPETTECode GJG·1983-04-28

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