Axsym Rea Ethanol
FDA 510(k) K953765 · Abbott Laboratories
510(k) numberK953765
Submission
- Device name
- Axsym Rea Ethanol
- Applicant
- Abbott Laboratories
Abbott Park, IL, US - Received
- August 11, 1995
- Decision date
- September 27, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DML – Nad-Nadh, Specific Reagent For Alcohol Enzyme Method
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3040
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DML
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K013538 | EthanolDML · Traditional | Abbott Laboratories | 12/14/2001SE |
| K993980 | Syva Emit II Plus Ethyl Alcohol Assay, Models 9K309UL/9K409ULDML · Traditional | Syva Co. | 02/01/2000SE |
| K963197 | On.Site AlcoholDML · Traditional | Ansys, Inc. | 09/19/1996SE |
| K952839 | Boehringer Mannheim Ethyl Alcohol AssayDML · Traditional | Boehringer Mannheim Corp. | 08/24/1995SE |
| K923337 | On*Site AlcoholDML · Traditional | Toxi-Lab, Inc. | 01/12/1993SE |
| K914777 | Sigma Procedure No. 333-UVDML · Traditional | Sigma Diagnostics, Inc. | 12/27/1991SE |
| K874382 | Raichem(Tm) Alcohol ReagentDML · Traditional | Reagents Applications, Inc. | 01/11/1988SE |
| K872180 | Kinetic 610 EthanolDML · Traditional | American Monitor Corp. | 07/07/1987SE |
| K863419 | Emds(Tm) Alcohol Testpacks, #67691/95DML · Traditional | Em Diagnostic Systems, Inc. | 09/29/1986SE |
| K840769 | Paramax Alcohol ReagentDML · Traditional | American Dade | 04/13/1984SE |
More from American Dade
| 510(k) | Device | Decision |
|---|---|---|
| K252424 | Anti-HCV NextMZO · Traditional | 04/28/2026SE |
| K243500 | ARCHITECT iGentamicinLCD · Special | 07/09/2025SE |
| K243168 | Alinity i Rubella IgGLFX · Traditional | 06/20/2025SE |
| K243283 | Alinity h-series SystemGKZ · Traditional | 02/20/2025SE |
| K233932 | Alinity i Toxo IgMLGD · Traditional | 08/30/2024SE |
| K232669 | TbiQAT · Special | 09/29/2023SE |
| K222850 | HAVAb IgG IILOL · Traditional | 08/10/2023SE |
| K220031 | Alinity h-series SystemGKZ · Traditional | 08/04/2023SE |
| K220282 | i-STAT PTplus Cartridge with the i-STAT 1 SystemGJS · Traditional | 07/14/2023SE |
| K230937 | Alinity i Total ß-hCG Reagent Kit, GLP systems TrackDHA · Traditional | 06/05/2023SE |
Questions and answers
When was Axsym Rea Ethanol cleared by the FDA?
Axsym Rea Ethanol (K953765) received a 510(k) decision of Substantially Equivalent on September 27, 1995, 47 days after the submission was received.
What is the product code of K953765?
The FDA product code is DML – Nad-Nadh, Specific Reagent For Alcohol Enzyme Method, a Class II (moderate risk) device regulated under 21 CFR 862.3040.