Drystar Axys XL
Catalogue number 5367/400, listed by Agfa Healthcare Inc., Canada, under Camera, Multi Format, Radiological. 2 manufacturers in China are registered for this product code.
Who Else Makes It
All of them in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Qisda Electronics (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 5 |
| Fujifilm Imaging System (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 3 |
Record
| Listed by | Agfa Healthcare Inc., Canada |
|---|---|
| FDA product code | LMC |
| Device type | Camera, Multi Format, Radiological |
| Device class | Class 2 |
| Regulation | 21 CFR 892.2040 |
| Establishment | Specification developer, Manufacturer |
| 510(k) | K072680 |
| Record published | 2016-09-01 |
| Record revised | 2019-06-14 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 5367/400 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Fuji Medical DRY Film | Fujifilm Corporation | 13 |
| Sony | Sony Corporation | 9 |
| Codonics Horizon® Multi-media Imager | Codonics, Inc. | 7 |
| Dryview 5700 Laser Imaging System | Carestream Health, Inc. | 4 |
| Dryview 5950 Laser Imaging System | Carestream Health, Inc. | 4 |
| Codonics Horizon® Operating Software | Codonics, Inc. | 4 |
| Drypro Model 873 | Konica Minolta, Inc. | 3 |
| Drypro Model 832 | Konica Minolta, Inc. | 2 |
| Drypix Plus | Fujifilm Corporation | 2 |
| Drypro Sigma | Konica Minolta, Inc. | 2 |
| Drypro Sigma 2 | Konica Minolta, Inc. | 2 |
| Dryview 6950 Laser Imaging System | Carestream Health, Inc. | 2 |
Showing 12 of 29. All products under Camera, Multi Format, Radiological
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K072680 | 2007-10-25 |
| K052251 | 2005-08-31 |
| K032635 | 2003-09-24 |
| K023287 | 2002-10-22 |
| K022658 | 2002-09-06 |
| K012941 | 2001-11-29 |
| K012010 | 2001-09-20 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Agfa Healthcare Inc. | 510(k) number | 2008-05-16 | Not classified | Other | The “Film Calibration” setting on the printers was set to the default “OFF” position instead of “ON”. | 33 units | 2008-10-10 |
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 |
|---|---|---|---|---|---|
| 2003-11-25 | Not classified | Other | The GS1 circuit board may fail resulting in smoke or fire. | The units were distributed to hospitals and other health fac | 2004-10-01 |
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.