Rep 3 Quto-Flur CHOLESTEROL-30
FDA 510(k) K962914 · Helena Laboratories
510(k) numberK962914
Submission
- Device name
- Rep 3 Quto-Flur CHOLESTEROL-30
- Applicant
- Helena Laboratories
Beaumont, TX, US - Received
- July 26, 1996
- Decision date
- January 13, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- JHO – Electrophoretic Separation, Lipoproteins
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1475
- Specialty
- Clinical Chemistry
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|---|---|---|---|
| K022333 | Spife LIPPOROTEIN-12, Model 3344JHO · Traditional | Helena Laboratories | 08/15/2002SE |
| K022053 | Hydragel 7 Lipoprotein(E), PN 4114 & Hydragel Lipoprotein(E) 15/30 PN 4134JHO · Special | Sebia | 07/12/2002SE |
| K013662 | Modification to Lipoprint System, LDL SubfractionsJHO · Special | Quantimetrix Corp. | 03/08/2002SE |
| K012789 | Modified to Ldl/Hdl Chol Direct Kit-P.N. 4005, 4103,4123JHO · Special | Morax | 01/17/2002SE |
| K013466 | Spife 2000/3000 Lipoprotein; Model# 3340, 3341, 3342, 3343JHO · Traditional | Helena Laboratories | 12/21/2001SE |
| K010337 | Lipoprint System, LDL SubfractionsJHO · Traditional | Quantimetrix Corp. | 07/25/2001SE |
| K000603 | Spife Cholesterol Profile KitJHO · Traditional | Helena Laboratories | 04/17/2000SE |
| K992971 | Rep Cholesterol Profile KitJHO · Traditional | Helena Laboratories | 10/18/1999SE |
| K974854 | Hydragel-Mini Lipo Kit-Pn 4093, Hydragel Lipo Kit-Pn 4007, Hydragel Lipo Maxi Kit-Pn 4207JHO · Traditional | Morax | 10/07/1998SE |
| K980650 | Rep Cholesterol Profile TEMPLATE-30, -16, -8; Rep Vis CholesterolJHO · Traditional | Helena Laboratories | 05/01/1998SE |
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Questions and answers
When was Rep 3 Quto-Flur CHOLESTEROL-30 cleared by the FDA?
Rep 3 Quto-Flur CHOLESTEROL-30 (K962914) received a 510(k) decision of Substantially Equivalent on January 13, 1997, 171 days after the submission was received.
What is the product code of K962914?
The FDA product code is JHO – Electrophoretic Separation, Lipoproteins, a Class I (low risk) device regulated under 21 CFR 862.1475.