Seragen Diagnostics, Inc.
Seragen Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1987.
Top product codes for Seragen Diagnostics, Inc.
Recent clearances by Seragen Diagnostics, Inc.
- K872148 — VIVID CHLAMYDIA(TM)
- K851663 — QUICK-COUNT HEMATOLOGY CONTROLS
- K852260 — QUICK-CHEM CALIBRATION SET
- K851520 — CK/LD ISOENZYMES CONTROLS(HUMAN)
- K851521 — LD-1(IMMUNO) SEPARATION SET
- K850209 — QUICK-LYTE
- K844743 — SERATEST ENA(RNP/SM) DETERMINATION
- K842563 — SERATEST DNA DETERMINATION
- K841504 — QUICK-COUNT PLUS 2
- K840793 — CK/MB IMMUNO-ISOENZYME CONTROL SERUM
- K840863 — SERATEST RF LATEX DETERMINATION
- K834396 — DIRECT IRON REAGENT SET
- K833972 — QUICK-COUNT HEMATOLOGY REAGENT KIT
- K833971 — QUICK-COUNT
- K833744 — ALKALINE PHOSPHATASE-RATE
- K833931 — UREA NITROGEN-UV
- K832926 — ENZYMATIC GLUCOSE DETERMINATION
- K832759 — TOTAL IRON-BINDING CAPACITY ACCESORY
- K831525 — H-FLU B ELISA TEST
- K822115 — SERAGAN ACTH125 I-RIA KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.