Technia Diagnostics , Ltd.

Technia Diagnostics , Ltd. holds 9 FDA 510(k) medical device clearances, first cleared 1979, most recent 1986.

Top product codes for Technia Diagnostics , Ltd.

Recent clearances by Technia Diagnostics , Ltd.

K861978 — AUTOFLUOR VCode KTL·1986-06-10
K801843 — T3(125) RADIOIMMUNOASSAY KITCode CDP·1980-09-16
K801202 — DIGOXIN RADIOIMMUNOASSAY KITCode LCS·1980-06-20
K801203 — CORTISOL RADIOIMMUNOASSAY KITCode CGR·1980-06-09
K791361 — T3 UPTAKE RADIOIMMUNOASSAY KITCode KHQ·1979-08-16
K790919 — HPL RIA KITCode JMF·1979-06-28
K790495 — THYROXINE RIA KITCode CDX·1979-05-03
K782024 — RIA KIT, VITAMIN B12Code CDD·1979-02-28
K782025 — GENTAMICIN FLUROIMMUNASSAY KITCode LCQ·1979-01-26

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