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FDA 510(k)

LEVO COMBI

K-Number: K030893 · 2003-04-02

ApplicantLevo AG
Decision Date2003-04-02
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVO COMBI is the device name listed in this FDA 510(k) record. The listed applicant is Levo AG. It received FDA 510(k) clearance on 2003-04-02 under 510(k) number K030893. 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 COMBI?

LEVO COMBI is a medical device that received FDA 510(k) clearance on 2003-04-02. The listed applicant is Levo AG. The 510(k) number is K030893.

When did LEVO COMBI receive FDA 510(k) clearance?

LEVO COMBI received FDA 510(k) clearance on 2003-04-02, under 510(k) number K030893.

Who is the listed applicant for LEVO COMBI?

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

What is the FDA product code for LEVO COMBI?

The FDA product code for LEVO COMBI 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.

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Other records listing Levo AG 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.

K083017LEVO C3K051387LEVO COMFORT II

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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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