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FDA 510(k)

LEVO ACTIVE-EASY LAE

K-Number: K971873 · 1997-07-03

ApplicantLevo USA
Decision Date1997-07-03
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVO ACTIVE-EASY LAE is the device name listed in this FDA 510(k) record. The listed applicant is Levo USA. It received FDA 510(k) clearance on 1997-07-03 under 510(k) number K971873. 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 ACTIVE-EASY LAE?

LEVO ACTIVE-EASY LAE is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Levo USA. The 510(k) number is K971873.

When did LEVO ACTIVE-EASY LAE receive FDA 510(k) clearance?

LEVO ACTIVE-EASY LAE received FDA 510(k) clearance on 1997-07-03, under 510(k) number K971873.

Who is the listed applicant for LEVO ACTIVE-EASY LAE?

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 ACTIVE-EASY LAE?

The FDA product code for LEVO ACTIVE-EASY LAE 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 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.

K963817LEVO MOBIL LCMK973951LEVO COMPACT-EASY LCEK963816LEVO COMPACT LC

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.

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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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