High Pressure Liquid Chromatography System
FDA 510(k) K872582 · Millipore Corp.
510(k) numberK872582
Submission
- Device name
- High Pressure Liquid Chromatography System
- Applicant
- Millipore Corp.
Milford, MA, US - Received
- June 30, 1987
- Decision date
- July 16, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LDM – Instrumentation, High Pressure Liquid Chromatography
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2260
- Specialty
- Clinical Chemistry
Other 510(k)s with product code LDM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K960392 | CDMLDM · Traditional | Bio-Rad | 07/08/1996SE |
| K961557 | Alliance 2690 Separations ModuleLDM · Traditional | Waters Corporation | 07/05/1996SE |
| K942451 | Bio-Rad Clinical Data Management SystemLDM · Traditional | Bio-Rad | 11/10/1994SE |
| K922388 | Waters(Tm) LC Module I for Clinical UseLDM · Traditional | Millipore Corp. | 09/11/1992SE |
| K920136 | Waters 717 AutosamplerLDM · Traditional | Millipore Corp. | 02/19/1992SE |
| K903647 | Module 486 Variable Wavelength Tunable Uv/Vis DeteLDM · Traditional | Millipore Corp. | 09/11/1990SE |
| K884886 | Model 250 Liquid Chromotagraphy PumpLDM · Traditional | The Perkin-Elmer Corp. | 02/02/1989SE |
| K870949 | Waters 650 Advanced Protein Purification SystemLDM · Traditional | Millipore Corp. | 04/22/1987SE |
| K862178 | Isopure LC SystemLDM · Traditional | The Perkin-Elmer Corp. | 07/14/1986SE |
| K850272 | Waters 740 Data Module-Plotter IntegratorLDM · Traditional | Millipore Corp. | 03/06/1985SE |
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| K013988 | Millex GP Sterilizing Filter Unit, Model SLGP 033 RBSN · Special | 04/04/2002SE |
| K963717 | Millex - MP Filter Unit (SLMPO25SS/SLMPL25SS)BSN · Traditional | 06/10/1997SE |
| K941326 | Ultrafree-ClJJH · Traditional | 05/27/1994SE |
| K934069 | Millex, Dualex (Plus, Ultra)FIB · Traditional | 04/21/1994SE |
| K924347 | Waters(Tm) 996 PdaKIE · Traditional | 12/11/1992SE |
| K922388 | Waters(Tm) LC Module I for Clinical UseLDM · Traditional | 09/11/1992SE |
| K920136 | Waters 717 AutosamplerLDM · Traditional | 02/19/1992SE |
Questions and answers
When was High Pressure Liquid Chromatography System cleared by the FDA?
High Pressure Liquid Chromatography System (K872582) received a 510(k) decision of Substantially Equivalent on July 16, 1987, 16 days after the submission was received.
What is the product code of K872582?
The FDA product code is LDM – Instrumentation, High Pressure Liquid Chromatography, a Class I (low risk) device regulated under 21 CFR 862.2260.