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FDA 510(k)

LIDO LINEA

K-Number: K903429 · 1990-08-14

ApplicantLoredan Biomedical, Inc.
Decision Date1990-08-14
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIDO 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 1990-08-14 under 510(k) number K903429. The device is classified under product code IKK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIDO LINEA?

LIDO LINEA is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K903429.

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

LIDO LINEA received FDA 510(k) clearance on 1990-08-14, under 510(k) number K903429.

Who is the listed applicant for LIDO 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 LINEA?

The FDA product code for LIDO LINEA is IKK.

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-TAKK924513LIDO(R) LINEAK884487LIDO TM ACTIVE BACKK880018LIDO(TM) WORKSETK880017LIDO(TM) LIFTK871793LIDO ACTIVE

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Related Devices (Code: IKK)

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.

K123746AMES THERAPY DEVICEAmes Technology, Inc.K952090HUMAC SYSTEMComputer Sports Medicine, Inc.K951770BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3APBiodex Medical Systems, Inc.K951916CC RIDER, MODEL ME180Mettler Electronics Corp.K950095CYBEX 770CybexK942229MOTIVATOR FTR 2000Hogan & Hartson

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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