Kronus Market Development Associates, Inc.
Kronus Market Development Associates, Inc. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2014.
Top product codes for Kronus Market Development Associates, Inc.
Recent clearances by Kronus Market Development Associates, Inc.
- DEN140001 — ZINC TRANSPORTER 8 ANTIBODY (ZNT8AB) ELISA ASSAY KIT
- K121046 — STEROID 21-HYDROXYLASE ANTIBODY (21-OHAB) RIA ASSAY KIT
- K111956 — KRONUS VOLTAGE GATED CALCIUM CHANNEL (VGCC) ANTIBODY RIA ASSAY KIT
- K080523 — KRONUS BLOCKING ACETYLCHOLINE RECEPTOR AUTOANTIBODY (ACHRAB) RIA ASSAY KIT
- K080159 — KRONUS TSH RECEPTOR AUTOANTIBODY (TRAB) ELISA ASSAY KIT
- K073590 — KRONUS IA-2 AUTOANTIBODY RIA ASSAY KIT
- K072135 — KRONUS GAD AUTOANTIBODY ELISA ASSAY KIT
- K070183 — KRONUS INSULIN AUTOANTIBODY (IAA) ASSAY KIT
- K051061 — KRONUS GLUTAMIC ACID DECARBOXYLASE ANTIBODY KIT
- K042248 — KRONUS, INC.'S ACETYLCHOLINE RECEPTOR ANTIBODY (ACHRAB) ASSAY KIT
- K032134 — TSH RECEPTOR ANTIBODY (TRAB) COATED TUBE (CT) ASSAY KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.