Lumiquick Diagnostics, Inc.
Lumiquick Diagnostics, Inc. holds FDA 510(k) medical device clearance, cleared in 2013, with 80 FDA device recalls on record.
Top product codes for Lumiquick Diagnostics, Inc.
FDA recalls by Lumiquick Diagnostics, Inc.
10 most recent of 80- Z-1392-2014 — Ketamine Strip; LumiQuick,. Santa Clara, CA 95054
- Z-1401-2014 — Methylphenidate Test Strip; LumiQuick,. Santa Clara, CA 95054
- Z-1359-2014 — Dengue NS1 Ag/IgG/M Ab Duo Test Card; LumiQuick. Santa Clara, CA 95054
- Z-1366-2014 — Tramadol Strip; LumiQuick. Santa Clara, CA 95054
- Z-1343-2014 — Salmonella typhi Antigen Test Card; LumiQuick, Santa Clara, CA 95054
- Z-1391-2014 — THC Test Card; LumiQuick,. Santa Clara, CA 95054
- Z-1384-2014 — Morphine Strip (300); LumiQuick, Santa Clara, CA 95054
- Z-1362-2014 — PSA Test Card (Whole Blood); LumiQuick. Santa Clara, CA 95054
- Z-1344-2014 — Rotavirus Test Card LumiQuick, Santa Clara, CA 95054
- Z-1416-2014 — CK-MB Test Card (Whole Blood); LumiQuick,. Santa Clara, CA 95054
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Lumiquick Diagnostics, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.