LEVO MOBIL LCM
K-Number: K963817 · 1997-12-23
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Device Summary
Frequently Asked Questions
What is the LEVO MOBIL LCM?
LEVO MOBIL LCM is a medical device that received FDA 510(k) clearance on 1997-12-23. The listed applicant is Levo USA. The 510(k) number is K963817.
When did LEVO MOBIL LCM receive FDA 510(k) clearance?
LEVO MOBIL LCM received FDA 510(k) clearance on 1997-12-23, under 510(k) number K963817.
Who is the listed applicant for LEVO MOBIL LCM?
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 MOBIL LCM?
The FDA product code for LEVO MOBIL LCM 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
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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