LIDO BACK— 510(k) K861986

Substantially Equivalent

Loredan Biomedical, Inc.

FDA 510(k) clearance K861986 for LIDO BACK, Substantially Equivalent on 1986-06-02. 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: 1986-05-22
Decision date: 1986-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Davis, CA, US

Download summary PDF View on FDA.gov ↗

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