Medical Device Manufacturer · US , Crofton , MD

Larsen & Toubro Limited - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2003

Recent clearances: STAR 50 N, STELLAR 300, STELLAR 300

18

Total

18

Cleared

0

Denied

FDA 510(k) Regulatory Record - Larsen & Toubro Limited Cardiovascular ✕

17 devices

1-12 of 17

Cleared Mar 15, 2011

Cardiovascular · 88d

Cleared CT Mar 11, 2011

Cardiovascular · 78d

Cleared CT Apr 29, 2010

Cardiovascular · 212d

Cleared Nov 20, 2009

SKYLINE 55, MODEL VER 1

Cardiovascular · 127d

Cleared Jun 05, 2009

STAR 55 MODEL 100

Cardiovascular · 133d

Cleared Jun 05, 2009

PLANET 55, MODEL 100

Cardiovascular · 105d

Cleared Sep 26, 2008

Cardiovascular · 11d

Cleared Jul 31, 2008

Cardiovascular · 58d

Cleared Feb 08, 2008

Cardiovascular · 15d

Cleared Sep 21, 2007

Cardiovascular · 115d

Cleared Jul 12, 2006

Cardiovascular · 14d

Cleared Jan 20, 2006

Cardiovascular · 11d

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Sep 01, 2026