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FDA 510(k)

STELLAR 404T

K-Number: K060058 · 2006-01-20

ApplicantLarsen & Toubro Limited
Decision Date2006-01-20
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STELLAR 404T 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 2006-01-20 under 510(k) number K060058. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STELLAR 404T?

STELLAR 404T is a medical device that received FDA 510(k) clearance on 2006-01-20. The listed applicant is Larsen & Toubro Limited. The 510(k) number is K060058.

When did STELLAR 404T receive FDA 510(k) clearance?

STELLAR 404T received FDA 510(k) clearance on 2006-01-20, under 510(k) number K060058.

Who is the listed applicant for STELLAR 404T?

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 STELLAR 404T?

The FDA product code for STELLAR 404T is MWI.

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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: MWI)

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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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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