Sterling Diagnostic Imaging, Inc.
Newark, DE, US
Sterling Diagnostic Imaging, Inc. appears in FDA device records in Newark, DE. FDA records list 7 510(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
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Sterling Diagnostic Imaging, Inc. between 1996 and 1998. The busiest year on record is 1997, with 4. The most recent is 1998, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1996 | 1 |
| 1997 | 4 |
| 1998 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K980970 | IIRAD DIRECTRAY OPERATOR CONSOLE | LLZ | Substantially Equivalent | |
| K980220 | IISYS PACS SYSTEM | LMD | Substantially Equivalent | |
| K974423 | ULTRA-VISION MAMMOGRAPHY DETAIL, ULTRA-VISION MAMMOGRAPHY FAST DETAIL | EAM | Substantially Equivalent | |
| K973206 | STERLING DIAGNOSTIC IMAGING DIRECT RADIOGRAPHY | MQB | Substantially Equivalent | |
| K972660 | RAVEN DRY PRINTER | LMC | Substantially Equivalent | |
| K973028 | HELIOS LASER IMAGER 1417 | LMC | Substantially Equivalent | |
| K964250 | LINX NETWORKING SYSTEM | LMD | 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