FDA 510(k)

LIDO V-TAK

K-Number: K924512 · 1993-05-12

Decision Date1993-05-12

Product CodeLXJ

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

LIDO V-TAK is the device name listed in this FDA 510(k) record. The listed applicant is Loredan Biomedical, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K924512. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDO V-TAK?

LIDO V-TAK is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K924512.

When did LIDO V-TAK receive FDA 510(k) clearance?

LIDO V-TAK received FDA 510(k) clearance on 1993-05-12, under 510(k) number K924512.

Who is the listed applicant for LIDO V-TAK?

The FDA 510(k) record lists Loredan Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIDO V-TAK?

The FDA product code for LIDO V-TAK is LXJ.

Other records listing Loredan Biomedical, Inc. 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.

K924513LIDO(R) LINEA K903429LIDO LINEA K884487LIDO TM ACTIVE BACK K880018LIDO(TM) WORKSET K880017LIDO(TM) LIFT K871793LIDO ACTIVE

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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.