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FDA 510(k)

LERADO, COSCO

K-Number: K050290 · 2005-02-18

ApplicantLerado Oversea Ltd. Twn Branch (Bvi)
Decision Date2005-02-18
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LERADO, COSCO is the device name listed in this FDA 510(k) record. The listed applicant is Lerado Oversea Ltd. Twn Branch (Bvi). It received FDA 510(k) clearance on 2005-02-18 under 510(k) number K050290. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LERADO, COSCO?

LERADO, COSCO is a medical device that received FDA 510(k) clearance on 2005-02-18. The listed applicant is Lerado Oversea Ltd. Twn Branch (Bvi). The 510(k) number is K050290.

When did LERADO, COSCO receive FDA 510(k) clearance?

LERADO, COSCO received FDA 510(k) clearance on 2005-02-18, under 510(k) number K050290.

Who is the listed applicant for LERADO, COSCO?

The FDA 510(k) record lists Lerado Oversea Ltd. Twn Branch (Bvi) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LERADO, COSCO?

The FDA product code for LERADO, COSCO is IOR.

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Other records listing Lerado Oversea Ltd. Twn Branch (Bvi) as applicant

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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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