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FDA 510(k)

STARSHIELD V3 RF TRNT

K-Number: K050237 · 2005-03-18

Decision Date2005-03-18
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

STARSHIELD V3 RF TRNT is the device name listed in this FDA 510(k) record. The listed applicant is Odin Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2005-03-18 under 510(k) number K050237. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STARSHIELD V3 RF TRNT?

STARSHIELD V3 RF TRNT is a medical device that received FDA 510(k) clearance on 2005-03-18. The listed applicant is Odin Medical Technologies , Ltd.. The 510(k) number is K050237.

When did STARSHIELD V3 RF TRNT receive FDA 510(k) clearance?

STARSHIELD V3 RF TRNT received FDA 510(k) clearance on 2005-03-18, under 510(k) number K050237.

Who is the listed applicant for STARSHIELD V3 RF TRNT?

The FDA 510(k) record lists Odin Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STARSHIELD V3 RF TRNT?

The FDA product code for STARSHIELD V3 RF TRNT is LNH.

Related Clinical Trials

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.

Other records listing Odin Medical Technologies , Ltd. 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.

Related Devices (Code: LNH)

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.

Official Source

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

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