Microgenics Corp.

Microgenics Corp. holds 107 FDA 510(k) medical device clearances, first cleared 1985, most recent 2013, with 2 FDA device recalls on record.

Clearances by Microgenics Corp. — page 2

101–107 of 107

K884358 — CEDIA THEOPHYLLINE ASSAYCode KLS·1989-02-07
K884634 — MODIFIED CEDIA TOTAL T4 ASSAYCode KLI·1988-12-09
K884054 — MODIFICATION OF THE CEDIA DIGOXIN ASSAYCode KXT·1988-12-02
K872583 — CEDIA DIGOXIN CR ASSAYCode KXT·1987-08-28
K872447 — CEDIA(TM) T UPTAKECode KHQ·1987-08-21
K854638 — CEDIA DIGOXIN ASSAYCode KXT·1986-03-25
K852164 — CEDIA TOTAL T4 ASSAYCode KLI·1985-07-22

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