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FDA 510(k)

LEVO COMPACT LC

K-Number: K963816 · 1996-10-30

ApplicantLevo USA
Decision Date1996-10-30
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVO COMPACT LC is the device name listed in this FDA 510(k) record. The listed applicant is Levo USA. It received FDA 510(k) clearance on 1996-10-30 under 510(k) number K963816. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVO COMPACT LC?

LEVO COMPACT LC is a medical device that received FDA 510(k) clearance on 1996-10-30. The listed applicant is Levo USA. The 510(k) number is K963816.

When did LEVO COMPACT LC receive FDA 510(k) clearance?

LEVO COMPACT LC received FDA 510(k) clearance on 1996-10-30, under 510(k) number K963816.

Who is the listed applicant for LEVO COMPACT LC?

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

What is the FDA product code for LEVO COMPACT LC?

The FDA product code for LEVO COMPACT LC is IPL.

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 Levo USA 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: IPL)

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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