Pausch Corp.
Tenton Falls, NJ, US
Pausch Corp. appears in FDA device records in Tenton Falls, NJ. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Pausch Corp. between 1979 and 2008. The busiest year on record is 1979, with 4. The most recent is 2008, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 4 |
| 1987 | 1 |
| 1990 | 1 |
| 1998 | 2 |
| 2008 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K081073 | HDR VISION, VISION HDR, HD R/F, UROMAT HD R/F | OWB | Substantially Equivalent | |
| K973864 | COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMO | IZF | Substantially Equivalent | |
| K973834 | CS2000 & CS2000 TOMO | IZF | Substantially Equivalent | |
| K903395 | UROMAT 2000 | IXR | Substantially Equivalent | |
| K870856 | COSMOS | IYB | Substantially Equivalent | |
| K790742 | KS-78 VERTICAL WALL CASSETTE HOLDER | IXY | Substantially Equivalent | |
| K790741 | COMPACT SYSTEM | KPR | Substantially Equivalent | |
| K790740 | BS 66, UNIVERSAL BUCKY STAND | KPR | Substantially Equivalent | |
| K790743 | COORDINATUS, HORIZONTAL RADIOGRAPHOC | KXJ | 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