LIDO(TM) WORKSET— 510(k) K880018

Substantially Equivalent

Loredan Biomedical, Inc.

FDA 510(k) clearance K880018 for LIDO(TM) WORKSET, Substantially Equivalent on 1988-02-26. Applicant: Loredan Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Loredan Biomedical, Inc.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1988-01-05
Decision date: 1988-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Davis, CA, US

Download summary PDF View on FDA.gov ↗

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