Samsung Mobile Display Co., Ltd.
Houston, TX, US
Samsung Mobile Display Co., Ltd. appears in FDA device records in Houston, TX. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Samsung Mobile Display Co., Ltd. between 2009 and 2011. The busiest year on record is 2011, with 3. The most recent is 2011, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2009 | 1 |
| 2010 | 1 |
| 2011 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K112751 | SDX-4343CS | MQB | Substantially Equivalent | |
| K112558 | DIGITAL FLAT PANEL X-RAY DETECTOR | MQB | Substantially Equivalent | |
| K102321 | DIGITAL FLAT PANEL X-RAY DETECTOR MODEL SDX-4336CP | MQB | Substantially Equivalent | |
| K102587 | LLX240AB01 | MQB | Substantially Equivalent | |
| K090742 | DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A | MQB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain