Double Antibody Ultra-Pth #KPTD1 and KPTD2
FDA 510(k) K871970 · Diagnostic Products Corp.
510(k) numberK871970
Submission
- Device name
- Double Antibody Ultra-Pth #KPTD1 and KPTD2
- Applicant
- Diagnostic Products Corp.
Los Angeles, CA, US - Received
- May 21, 1987
- Decision date
- September 25, 1987
- 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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| 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 |
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Questions and answers
When was Double Antibody Ultra-Pth #KPTD1 and KPTD2 cleared by the FDA?
Double Antibody Ultra-Pth #KPTD1 and KPTD2 (K871970) received a 510(k) decision of Substantially Equivalent on September 25, 1987, 127 days after the submission was received.
What is the product code of K871970?
The FDA product code is CEW – Radioimmunoassay, Parathyroid Hormone, a Class II (moderate risk) device regulated under 21 CFR 862.1545.