LLOYD LINDEN, MODEL E04— 510(k) K071761

Substantially Equivalent

Lloyd Linden, Inc.

FDA 510(k) clearance K071761 for LLOYD LINDEN, MODEL E04, Substantially Equivalent on 2007-08-03. Applicant: Lloyd Linden, Inc.. Device class: 2.

Clearance details

Applicant: Lloyd Linden, Inc.
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 2007-06-29
Decision date: 2007-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Banqiao, Taipei County, TW

Download summary PDF View on FDA.gov ↗

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