Architect
Activated Aspartate Aminotransferase
2manufacturers in China registered for this device type
3catalogue numbers in this listing
8510(k) clearances naming this product code
1recall
Who Else Makes It
Concentrated in Jilin (1), Shandong (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Dirui Industrial Co., Ltd. | Changchun | Jilin | Contract manufacturer | 84 |
| Biobase Biodustry(Shandong)Co., Ltd. | Jinan | Shandong | Manufacturer | 70 |
Record
| Listed by | Abbott Laboratories, United States |
|---|---|
| FDA product code | CIT |
| Device type | Nadh Oxidation/Nad Reduction, Ast/Sgot |
| Device class | Class 2 |
| Regulation | 21 CFR 862.1100 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2016-09-09 |
| Record revised | 2024-02-21 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Storage environment temperature 2 to 8 °C; Handling environment temperature up to 29 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 7D81-21 | In distribution | |
| 8L91-21 | In distribution | |
| 8L91-41 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Biobase | Biobase Biodustry(Shandong)Co., Ltd. | 19 |
| AST | Randox Laboratories Limited | 10 |
| JAS Diagnostics | Drew Scientific, Ltd. | 7 |
| Synermed® | Infrared Laboratory Systems LLC | 7 |
| Pointe Scientific, Inc. | Horiba Instruments Incorporated | 5 |
| AU | Beckman Coulter, Inc. | 4 |
| Architect | Abbott Ireland | 4 |
| Synchron | Beckman Coulter, Inc. | 4 |
| ACE | Alfa Wassermann | 4 |
| Architect | Abbott Medical | 3 |
| Alinity | Abbott Ireland | 3 |
| Aspartate aminotransferase acc to Ifcc withwithout pyridoxal phosphate activat | Roche Diagnostics Gmbh | 3 |
Showing 12 of 62. All products under Nadh Oxidation/Nad Reduction, Ast/Sgot
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K071525 | 2008-03-19 |
| K983131 | 1998-09-28 |
| K981843 | 1998-06-29 |
| K981225 | 1998-04-23 |
| K981221 | 1998-04-23 |
| K894180 | 1989-09-13 |
| K860465 | 1986-05-05 |
| K854982 | 1986-01-14 |
Recalls
The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2008-06-30 | Not classified | Nonconforming Material/Component | This letter is to inform you that some samples may generate A-AST results of less than (<) 5 U/L or results within the reference range when actual concentration exceeds the non-Flex linearity of 1985 U/L. In other cases the following error | 1,646 | 2012-04-23 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.