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FDA 510(k)

LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM

K-Number: K040409 · 2004-02-27

ApplicantLarsen & Toubro Limited
Decision Date2004-02-27
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Larsen & Toubro Limited. It received FDA 510(k) clearance on 2004-02-27 under 510(k) number K040409. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM?

LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 2004-02-27. The listed applicant is Larsen & Toubro Limited. The 510(k) number is K040409.

When did LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM receive FDA 510(k) clearance?

LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM received FDA 510(k) clearance on 2004-02-27, under 510(k) number K040409.

Who is the listed applicant for LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM?

The FDA 510(k) record lists Larsen & Toubro Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM?

The FDA product code for LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM is IYN.

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Other records listing Larsen & Toubro Limited as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K103686STAR 50 NK103763STELLAR 300K093017STELLAR 300K092153SKYLINE 55, MODEL VER 1K090172STAR 55 MODEL 100K090443PLANET 55, MODEL 100

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Related Devices (Code: IYN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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