Advia Ims Carbamazepine Method
FDA 510(k) K042808 · Bayer Healthcare, LLC
510(k) numberK042808
Submission
- Device name
- Advia Ims Carbamazepine Method
- Applicant
- Bayer Healthcare, LLC
Tarrytown, NY, US - Received
- October 12, 2004
- Decision date
- February 8, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KLT – Enzyme Immunoassay, Carbamazepine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3645
- Specialty
- Clinical Toxicology
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| K031902 | Online TDM CarbamazepineKLT · Traditional | Roche Diagnostics Corp. | 09/17/2003SE |
| K011648 | Randox CarbamazepineKLT · Traditional | Randox Laboratories, Ltd. | 01/15/2002SE |
| K010814 | Emit 2000 Carbamazepine Assay, Model OSR4F229KLT · Special | Syva Co., Dade Behring, Inc. | 04/13/2001SE |
| K000903 | Additional Assays for Bayer Advia Ims SystemKLT · Traditional | Bayer Corp. | 05/18/2000SE |
| K000007 | Immulite Carbamazepine, Immulite 2000 Carbamazepine, Catalog # LKCB1, LKCB5 & L2KCB2…KLT · Traditional | Diagnostic Products Corp. | 02/28/2000SE |
| K993987 | Syva Emit II Plus Barbiturate Assay, Model 9D029UL/9D129ULKLT · Traditional | Syva Co. | 01/27/2000SE |
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Questions and answers
When was Advia Ims Carbamazepine Method cleared by the FDA?
Advia Ims Carbamazepine Method (K042808) received a 510(k) decision of Substantially Equivalent on February 8, 2005, 119 days after the submission was received.
What is the product code of K042808?
The FDA product code is KLT – Enzyme Immunoassay, Carbamazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3645.