Larsen & Toubro Limited
Crofton, MD, US
Larsen & Toubro Limited appears in FDA device records in Crofton, MD. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Larsen & Toubro Limited between 2003 and 2011. The busiest year on record is 2008, with 3. The most recent is 2011, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2003 | 2 |
| 2004 | 2 |
| 2005 | 2 |
| 2006 | 2 |
| 2007 | 1 |
| 2008 | 3 |
| 2009 | 3 |
| 2010 | 1 |
| 2011 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K103686 | STAR 50 N | MWI | Substantially Equivalent | |
| K103763 | STELLAR 300 | MWI | Substantially Equivalent | |
| K093017 | STELLAR 300 | MWI | Substantially Equivalent | |
| K092153 | SKYLINE 55, MODEL VER 1 | MWI | Substantially Equivalent | |
| K090443 | PLANET 55, MODEL 100 | MHX | Substantially Equivalent | |
| K090172 | STAR 55 MODEL 100 | MHX | Substantially Equivalent | |
| K082685 | GALAXY 55 | MWI | Substantially Equivalent | |
| K081552 | SKYLINE 55 | MWI | Substantially Equivalent | |
| K080173 | STAR 55 | MWI | Substantially Equivalent | |
| K071472 | PLANET 55 | MWI | Substantially Equivalent | |
| K061816 | GALAXY | MWI | Substantially Equivalent | |
| K060058 | STELLAR 404T | MWI | Substantially Equivalent | |
| K051608 | STAR 50 MONITORING SYSTEM | MWI | Substantially Equivalent | |
| K043370 | PLANET 50 MONITORING SYSTEM | MWI | Substantially Equivalent | |
| K042560 | STELLAR 404 MONITORING SYSTEM | MWI | Substantially Equivalent | |
| K040409 | LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM | IYN | Substantially Equivalent | |
| K032871 | PLANET MONITORING SYSTEM | MWI | Substantially Equivalent | |
| K032867 | STAR (LUNAR SERIES) MONITORING SYSTEM | MWI | 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