Covidien, Formerly Valleylab, A Division of Tyco H
Boulder, CO, US
Covidien, Formerly Valleylab, A Division of Tyco H appears in FDA device records in Boulder, CO. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Covidien, Formerly Valleylab, A Division of Tyco H between 2011 and 2014. The busiest year on record is 2013, with 3. The most recent is 2014, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2011 | 1 |
| 2012 | 1 |
| 2013 | 3 |
| 2014 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K141371 | SONICISION CORDLESS ULTRASONIC DISSECTOR | LFL | Substantially Equivalent | |
| K133338 | LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX) | GEI | Substantially Equivalent | |
| K131170 | SONICISION STERILIZATION TRAY | KCT | Substantially Equivalent | |
| K123444 | LIGASURE IMPACT CURVED, LARGE JAW, OPEN SEALER / DIVIDER | GEI | Substantially Equivalent | |
| K113572 | LIGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER | GEI | Substantially Equivalent | |
| K102913 | FORCETRIAD | GEI | 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