Columnmate II GHB Affinity Regenerable Column
FDA 510(k) K946274 · Helena Laboratories
510(k) numberK946274
Submission
- Device name
- Columnmate II GHB Affinity Regenerable Column
- Applicant
- Helena Laboratories
Beaumont, TX, US - Received
- December 23, 1994
- Decision date
- July 11, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- LCP – Assay, Glycosylated Hemoglobin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.7470
- Specialty
- Hematology
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| K231465 | Q-Pad Test SystemLCP · Traditional | Qurasense | 12/06/2023SE |
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| K183230 | OneDraw A1C Test SystemLCP · Traditional | Drawbridge Health, Inc. | 08/15/2019SE |
| K181915 | PixoTest POCT System - PixoTest POCT Analyzer and PixoTest A1c Test KitLCP · Traditional | Ixensor Co, Ltd. | 04/12/2019SE |
| K180509 | Quo-Test A1c SystemLCP · Dual Track | Ekf-Diagnostic GmbH | 02/16/2019SE |
| K173127 | skyla Hi Hemoglobin A1c System (skyla Hi Analyzer and skyla Hi Hemoglobin A 1 c Reagent…LCP · Traditional | Skyla Corporation H.S.P.B | 09/25/2018SE |
| K170623 | ACE Hemoglobin A1c (HbA1c) ReagentLCP · Traditional | Alfa Wassermann Diagnostic Technologies, LLC | 02/27/2018SE |
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Questions and answers
When was Columnmate II GHB Affinity Regenerable Column cleared by the FDA?
Columnmate II GHB Affinity Regenerable Column (K946274) received a 510(k) decision of Substantially Equivalent on July 11, 1995, 200 days after the submission was received.
What is the product code of K946274?
The FDA product code is LCP – Assay, Glycosylated Hemoglobin, a Class II (moderate risk) device regulated under 21 CFR 864.7470.