Radioimmunoassay Parathyroid Hormone Mid
FDA 510(k) K821131 · Endocrine-Metabolic Center
510(k) numberK821131
Submission
- Device name
- Radioimmunoassay Parathyroid Hormone Mid
- Applicant
- Endocrine-Metabolic Center
Mchenry, IL, US - Received
- April 20, 1982
- Decision date
- June 2, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CEW – Radioimmunoassay, Parathyroid Hormone
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1545
- Specialty
- Clinical Chemistry
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|---|---|---|---|
| K231927 | Elecsys PTH , Elecsys PTH STATCEW · Traditional | Roche Diagnostics | 03/22/2024SE |
| K232791 | Access Intact PTHCEW · Traditional | Beckman Coulter, Inc. | 03/01/2024SE |
| K221197 | VITROS Immunodiagnostic Products Intact PTH II Reagent PackCEW · Traditional | Ortho Clinical Diagnostics | 09/05/2023SE |
| K190702 | Lumipulse G whole PTHCEW · Traditional | Fujirebio Diagnostics,Inc. | 08/30/2019SE |
| K163658 | ADVIA Centaur Intact Parathyroid Hormone (PTH) AssayCEW · Traditional | Siemens Healthcare Diagnostics, Inc. | 05/23/2017SE |
| K161158 | IDS-iSYS Intact PTHNCEW · Traditional | Immunodiagnostic Systems , Ltd. | 01/31/2017SE |
| K150879 | LIASON 1-84 PTH Assay, LIASON 1-84 PTH Control Set, LIASON 1-84 PTH Calibration VerifiersCEW · Traditional | DiaSorin, Inc. | 06/22/2015SE |
| K133601 | Advia Centaur Intact Parathyroid Hormone (Ipth) AssayCEW · Traditional | Siemens Healthcare Diagnostics, Inc. | 02/05/2014SE |
| K132515 | Liaison N-Tact PTH Gen II, Control Set, Calibration VerifiersCEW · Traditional | DiaSorin, Inc. | 11/08/2013SE |
| K121981 | Advia Centaur Inact Parathyroid Hormone (Ipth) AssayCEW · Traditional | Siemens Healthcare Diagnostics | 03/21/2013SE |
More from Siemens Healthcare Diagnostics
| 510(k) | Device | Decision |
|---|---|---|
| K811993 | Radioimmunoassay, Follicle StimulatingCGJ · Traditional | 08/03/1981SE |
| K811994 | Radioimmunoassay Luteinizing HormoneCEP · Traditional | 07/27/1981SE |
| K810948 | Radioimmunoassay Thyroid Stim. Horm. KitJLW · Traditional | 04/17/1981SE |
| K810351 | Radioimmunoassay, Total TriiodothronieCDP · Traditional | 02/23/1981SE |
| K800188 | EMC-M-180, T3 Uptake - 100 TubesKHQ · Traditional | 02/13/1980SE |
| K800187 | EMC-M-175, Thyroxine - 100 TubesCDX · Traditional | 02/13/1980SE |
| K790602 | Ria, DIGNXIN-125-IDPB · Traditional | 07/30/1979SE |
| K790630 | Ria, Insulin, Double AntibodyCFP · Traditional | 07/24/1979SE |
Questions and answers
When was Radioimmunoassay Parathyroid Hormone Mid cleared by the FDA?
Radioimmunoassay Parathyroid Hormone Mid (K821131) received a 510(k) decision of Substantially Equivalent on June 2, 1982, 43 days after the submission was received.
What is the product code of K821131?
The FDA product code is CEW – Radioimmunoassay, Parathyroid Hormone, a Class II (moderate risk) device regulated under 21 CFR 862.1545.