Bilirubin Calibrators & Control
FDA 510(k) K832094 · Gilford Diagnostics
510(k) numberK832094
Submission
- Device name
- Bilirubin Calibrators & Control
- Applicant
- Gilford Diagnostics
Mchenry, IL, US - Received
- June 28, 1983
- Decision date
- August 11, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JIT – Calibrator, Secondary
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1150
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JIT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K171168 | VITROS Immunodiagnostic Products Insulin CalibratorsJIT · Abbreviated | Ortho Clinical Diagnostics | 05/16/2017SE |
| K170938 | CalSet IGF-1JIT · Traditional | Roche Diagnostics | 04/26/2017SE |
| K170160 | Abbott ARCHITECT Free T3JIT · Traditional | Abbott Laboratories | 02/15/2017SE |
| K163546 | Lumipulse G Progesterone-N CalibratorsJIT · Abbreviated | Fujirebio Diagnostics,Inc. | 01/13/2017SE |
| K163534 | Lumipulse G FSH-N CalibratorsJIT · Abbreviated | Fujirebio Diagnostics,Inc. | 01/13/2017SE |
| K163544 | Lumipulse G ProlactinJIT · Abbreviated | Fujirebio Diagnostics,Inc. | 01/12/2017SE |
| K163521 | Lumipulse G LH CalibratorsJIT · Abbreviated | Fujirebio Diagnostics,Inc. | 01/12/2017SE |
| K163078 | Dc-Uibc-CalJIT · Abbreviated | Sekisui Diagnostics P.E.I., Inc. | 12/08/2016SE |
| K163053 | Lumipulse G E2-III CalibratorsJIT · Abbreviated | Fujirebio Diagnostics,Inc. | 12/01/2016SE |
| K162538 | ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) CalibratorJIT · Special | Siemens Healthcare Diagnostics | 11/17/2016SE |
More from Siemens Healthcare Diagnostics
| 510(k) | Device | Decision |
|---|---|---|
| K831844 | Direct Bilirubin ReagentCIG · Traditional | 07/18/1983SE |
| K831843 | Gilchem Total Bilirubin ReagentCIG · Traditional | 07/18/1983SE |
| K823709 | Triglyceride Reagent (UV)CDT · Traditional | 01/07/1983SE |
| K822739 | AhbdJMK · Traditional | 10/18/1982SE |
| K822334 | Bilirubin CalibratorsJIT · Traditional | 09/02/1982SE |
| K822289 | CO2/CI StandardsJIX · Traditional | 08/24/1982SE |
| K822149 | Gilchem Y-Gt ReagentJPZ · Traditional | 08/12/1982SE |
| K821719 | Ammonia ReagentJIF · Traditional | 06/24/1982SE |
| K820976 | Gil Chem Magnesium ReagentJGJ · Traditional | 04/26/1982SE |
| K820975 | Gilchem Acid Phosphatase ReagentCKB · Traditional | 04/26/1982SE |
Questions and answers
When was Bilirubin Calibrators & Control cleared by the FDA?
Bilirubin Calibrators & Control (K832094) received a 510(k) decision of Substantially Equivalent on August 11, 1983, 44 days after the submission was received.
What is the product code of K832094?
The FDA product code is JIT – Calibrator, Secondary, a Class II (moderate risk) device regulated under 21 CFR 862.1150.