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FDA 510(k)

LIDO ACTIVE

K-Number: K871793 · 1987-06-05

ApplicantLoredan Biomedical, Inc.
Decision Date1987-06-05
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIDO ACTIVE 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 1987-06-05 under 510(k) number K871793. 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 ACTIVE?

LIDO ACTIVE is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K871793.

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

LIDO ACTIVE received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871793.

Who is the listed applicant for LIDO ACTIVE?

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 ACTIVE?

The FDA product code for LIDO ACTIVE is IKK.

Related Clinical Trials

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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) LINEAK903429LIDO LINEAK884487LIDO TM ACTIVE BACKK880017LIDO(TM) LIFTK880018LIDO(TM) WORKSET

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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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