Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LIDO TM ACTIVE BACK

K-Number: K884487 · 1988-11-18

ApplicantLoredan Biomedical, Inc.
Decision Date1988-11-18
Product CodeIKK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIDO TM ACTIVE BACK 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 1988-11-18 under 510(k) number K884487. 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 TM ACTIVE BACK?

LIDO TM ACTIVE BACK is a medical device that received FDA 510(k) clearance on 1988-11-18. The listed applicant is Loredan Biomedical, Inc.. The 510(k) number is K884487.

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

LIDO TM ACTIVE BACK received FDA 510(k) clearance on 1988-11-18, under 510(k) number K884487.

Who is the listed applicant for LIDO TM ACTIVE BACK?

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 TM ACTIVE BACK?

The FDA product code for LIDO TM ACTIVE BACK 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 LINEAK880017LIDO(TM) LIFTK880018LIDO(TM) WORKSETK871793LIDO ACTIVE

View all 9 devices →

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.

↑