Amikacin Ria Kit
FDA 510(k) K802877 · Antibodies, Inc.
510(k) numberK802877
Submission
- Device name
- Amikacin Ria Kit
- Applicant
- Antibodies, Inc.
Mchenry, IL, US - Received
- November 17, 1980
- Decision date
- December 19, 1980
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KLQ – Radioimmunoassay, Amikacin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3035
- Specialty
- Clinical Toxicology
Other 510(k)s with product code KLQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K052815 | QMS Amikacin ReagentsKLQ · Traditional | Seradyn, Inc. | 11/01/2005SE |
| K033884 | Randox AmikacinKLQ · Traditional | Randox Laboratories, Ltd. | 06/09/2004SE |
| K955570 | Innofluor Amikacin Assay SystemKLQ · Traditional | Oxis Intl., Inc. | 02/09/1996SE |
| K903100 | Innofluor (TM) Amikacin Reagent SetKLQ · Traditional | Innotron of Oregon, Inc. | 08/09/1990SE |
| K894517 | FPR Amikacin KitKLQ · Traditional | Colony Laboratories, Inc. | 09/28/1989SE |
| K852317 | Cobas FP Reagen for Amikacin & Amikacin CalibratorKLQ · Traditional | Roche Diagnostic Systems, Inc. | 06/25/1985SE |
| K843211 | Amikacin Analytical Test Pack AcaKLQ · Traditional | E.I. Dupont DE Nemours & Co., Inc. | 09/12/1984SE |
| K841161 | Immpulse Amikacin Assay ReagentsKLQ · Traditional | Paragon Diagnostics, Inc. | 05/02/1984SE |
| K840193 | Emit QST Amikacin AssayKLQ · Traditional | Syva Co. | 03/23/1984SE |
| K832336 | Stratus Amikacin FluorometricKLQ · Traditional | American Dade | 08/31/1983SE |
More from American Dade
| 510(k) | Device | Decision |
|---|---|---|
| K890774 | Giardeia(Tm)KHW · Traditional | 04/04/1989SE |
| K843590 | Detect-A-StrepGTZ · Traditional | 10/30/1984SE |
| K822892 | Cortisol Ria KitCGR · Traditional | 11/01/1982SE |
| K812749 | Ultra-DigLCS · Traditional | 10/19/1981SE |
| K812314 | Crithidna Anti-Dna Test KitDHN · Traditional | 09/01/1981SE |
| K800743 | Tobramycin Ria KitKLB · Traditional | 04/16/1980SE |
| K791217 | TSH Ria KitJLW · Traditional | 09/04/1979SE |
| K781656 | Nephelrate Antiserums, IggCFN · Traditional | 11/08/1978SE |
| K781655 | Nephelrate Antiserums 1GACFN · Traditional | 11/08/1978SE |
| K781654 | Nephelrate Antiperums LGMCFN · Traditional | 11/08/1978SE |
Questions and answers
When was Amikacin Ria Kit cleared by the FDA?
Amikacin Ria Kit (K802877) received a 510(k) decision of Substantially Equivalent on December 19, 1980, 32 days after the submission was received.
What is the product code of K802877?
The FDA product code is KLQ – Radioimmunoassay, Amikacin, a Class II (moderate risk) device regulated under 21 CFR 862.3035.