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FDA 510(k)

LIDO(R) LINEA

K-Number: K924513 · 1993-03-31

ApplicantLoredan Biomedical, Inc.
Decision Date1993-03-31
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIDO(R) LINEA 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 1993-03-31 under 510(k) number K924513. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDO(R) LINEA?

LIDO(R) LINEA is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K924513.

When did LIDO(R) LINEA receive FDA 510(k) clearance?

LIDO(R) LINEA received FDA 510(k) clearance on 1993-03-31, under 510(k) number K924513.

Who is the listed applicant for LIDO(R) LINEA?

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(R) LINEA?

The FDA product code for LIDO(R) LINEA is BXB.

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 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.

K924512LIDO V-TAKK903429LIDO LINEAK884487LIDO TM ACTIVE BACKK880018LIDO(TM) WORKSETK880017LIDO(TM) LIFTK871793LIDO ACTIVE

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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