Hydragel Protein(E) Kit
FDA 510(k) K951536 · Sebia
510(k) numberK951536
Submission
- Device name
- Hydragel Protein(E) Kit
- Applicant
- Sebia
Chelsea, MI, US - Received
- April 3, 1995
- Decision date
- June 30, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- CEF – Electrophoretic, Protein Fractionation
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1630
- Specialty
- Clinical Chemistry
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| K972274 | SpifeCEF · Traditional | Helena Laboratories | 10/27/1997SE |
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| K963018 | Bio-Rad Serum Proteins by Capillary ElectrophoresisCEF · Traditional | Bio-Rad | 06/04/1997SE |
| K964453 | Rep 3 Flur SPE-60 KitCEF · Traditional | Helena Laboratories | 12/23/1996SE |
| K960029 | Hydrasys Agarose Gel Electrophoresis Apparatus/Hydragel 15,30 Protein KitCEF · Traditional | Morax | 07/17/1996SE |
| K930317 | Rep Spe Hi-Res Template System, Cat 3276/3277/3278CEF · Traditional | Helena Laboratories | 08/03/1993SE |
| K922053 | Rep Spe Plus (Ponceau S) SystemCEF · Traditional | Helena Laboratories | 08/18/1992SE |
| K922024 | Rep Spe Plus (Acid Blue) System,# 3173/3174/3175CEF · Traditional | Helena Laboratories | 07/23/1992SE |
| K913315 | Bio-Rad Total Protein Test KitCEF · Traditional | Bio-Rad | 01/02/1992SE |
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Questions and answers
When was Hydragel Protein(E) Kit cleared by the FDA?
Hydragel Protein(E) Kit (K951536) received a 510(k) decision of Substantially Equivalent on June 30, 1995, 88 days after the submission was received.
What is the product code of K951536?
The FDA product code is CEF – Electrophoretic, Protein Fractionation, a Class I (low risk) device regulated under 21 CFR 862.1630.