LIDO V-TAK— 510(k) K924512

Substantially Equivalent

Loredan Biomedical, Inc.

FDA 510(k) clearance K924512 for LIDO V-TAK, Substantially Equivalent on 1993-05-12. Applicant: Loredan Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Loredan Biomedical, Inc.
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 1992-09-04
Decision date: 1993-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

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