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FDA 510(k)

LADY COMP USA

K-Number: K050094 · 2006-04-20

ApplicantLady Comp USA
Decision Date2006-04-20
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

LADY COMP USA is the device name listed in this FDA 510(k) record. The listed applicant is Lady Comp USA. It received FDA 510(k) clearance on 2006-04-20 under 510(k) number K050094. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LADY COMP USA?

LADY COMP USA is a medical device that received FDA 510(k) clearance on 2006-04-20. The listed applicant is Lady Comp USA. The 510(k) number is K050094.

When did LADY COMP USA receive FDA 510(k) clearance?

LADY COMP USA received FDA 510(k) clearance on 2006-04-20, under 510(k) number K050094.

Who is the listed applicant for LADY COMP USA?

The FDA 510(k) record lists Lady Comp USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LADY COMP USA?

The FDA product code for LADY COMP USA is LHD.

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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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