LOI SYSTEM— 510(k) K090525

Substantially Equivalent

Palomar Medical Products, Inc.

FDA 510(k) clearance K090525 for LOI SYSTEM, Substantially Equivalent on 2009-06-01. Applicant: Palomar Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Palomar Medical Products, Inc.
Product code: Code ONG
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2009-02-26
Decision date: 2009-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.