In Vitro Diagnostics, Inc.
FDA 510(k) medical device clearances.
Top product codes for In Vitro Diagnostics, Inc.
Recent clearances by In Vitro Diagnostics, Inc.
- K896867 — THYROID STIMULATING HORMONE-EIA-XT
- K896863 — DIGOXIN-EIA-XT
- K896866 — LUTEINIZING HORMONE-EIA-XT
- K896865 — VITRO T4-EIA-XT
- K896925 — T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT
- K896864 — FOLLICLE STIMULATING HORMONE-EIA-XT
- K873832 — REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801
- K871182 — FLAME PHOTOMETER STANDARD #60081 120 NA/2K
- K871183 — FLAME PHOTOMETER STANDARD #60082 140 NA/5K
- K871184 — FLAME PHOTOMETER STANDARD #60083 160 NA/8K
- K871185 — LITHIUM INTERNAL STANDARD 1 MEQ/L #60085
- K871186 — CESIUM DILUENT 1.5 MMOL CS/L #60087
- K871187 — LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084
- K871188 — LITHIUM INTERNAL STANDARD 1500 MEQ/L #60086
- K853304 — 21 HEMATOLOGY REAGENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.