Verathon Incorporated
Bothell, WA, US
Verathon Incorporated appears in FDA device records in Bothell, WA. 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 Verathon Incorporated between 2007 and 2017. The busiest year on record is 2007, with 1. The most recent is 2017, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 1 |
| 2008 | 1 |
| 2009 | 1 |
| 2015 | 1 |
| 2017 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K172356 | BladderScan Prime PLUS System | IYO | Substantially Equivalent | |
| K153101 | BladderScan Prime System | IYO | Substantially Equivalent | |
| K090214 | VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND | IYO | Substantially Equivalent | |
| K082456 | VERATHON INC. BLADDERSCAN ULTRASOUND SYSTEM, MODEL BVI 9600 | IYO | Substantially Equivalent | |
| K071217 | BLADDERSCAN BVI 9400 ULTRASOUND | IYO | 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