LEKTROGEL, MODEL LK3001— 510(k) K030887

Substantially Equivalent

Inmed Ltda.

FDA 510(k) clearance K030887 for LEKTROGEL, MODEL LK3001, Substantially Equivalent on 2003-06-13. Applicant: Inmed Ltda.. Device class: 2.

Clearance details

Applicant: Inmed Ltda.
Product code: Code GYB
Device class: Class 2
Regulation: 21 CFR 882.1275
Advisory panel: Neurology
Date received: 2003-03-21
Decision date: 2003-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, 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.