In Vitro Diagnostics, Inc.
In Vitro Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1990.
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.