Total T3 Enzyme Immunoassay Test Kit, Model BC-1005
FDA 510(k) K991311 · Biocheck, Inc.
510(k) numberK991311
Submission
- Device name
- Total T3 Enzyme Immunoassay Test Kit, Model BC-1005
- Applicant
- Biocheck, Inc.
Northridge, CA, US - Received
- April 16, 1999
- Decision date
- June 2, 1999
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- CDP – Radioimmunoassay, Total Triiodothyronine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1710
- Specialty
- Clinical Chemistry
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| K001607 | Reprobead T3 Enzyme Immunoassay Reagent Kit (Catalog# 104)CDP · Traditional | Repromedix Corp. | 10/05/2000SE |
| K991692 | Chiron Diagnostics Acs: 180 FT3CDP · Traditional | Chiron Diagnostics Corp. | 06/18/1999SE |
| K991252 | Aia-Pack FT3 AssayCDP · Traditional | Tosoh Medics, Inc. | 05/11/1999SE |
| K981824 | Opticoat T3 Eia KitCDP · Traditional | Biotecx Laboratories, Inc. | 12/22/1998SE |
| K983439 | Abbott Architect Free T3CDP · Traditional | Abbott Laboratories | 11/20/1998SE |
| K983434 | Abbott Architect Total T3CDP · Traditional | Abbott Laboratories | 11/20/1998SE |
| K974027 | Auraflex FT3 150 Test Pack, Auraflex FT3 Calibrator PackCDP · Traditional | Alfa Biotech (Uk) , Ltd. | 02/02/1998SE |
| K974634 | Immulite Free T3CDP · Traditional | Diagnostic Products Corp. | 01/02/1998SE |
| K973966 | Access Total T3 Reagents on the Access Immunoassay AnalyzerCDP · Traditional | Beckman Instruments, Inc. | 10/31/1997SE |
| K971779 | Total TRIIODOTHYRONINE(T3) Microplate EiaCDP · Traditional | Monobind | 06/16/1997SE |
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Questions and answers
When was Total T3 Enzyme Immunoassay Test Kit, Model BC-1005 cleared by the FDA?
Total T3 Enzyme Immunoassay Test Kit, Model BC-1005 (K991311) received a 510(k) decision of Substantially Equivalent on June 2, 1999, 47 days after the submission was received.
What is the product code of K991311?
The FDA product code is CDP – Radioimmunoassay, Total Triiodothyronine, a Class II (moderate risk) device regulated under 21 CFR 862.1710.