LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001— 510(k) K031321

Name: FDA 510(k) clearance K031321
Creator: U.S. Food and Drug Administration
Published: 2004-01-21

Substantially Equivalent

Medlogic Global Limited

FDA 510(k) clearance K031321 for LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001, Substantially Equivalent on 2004-01-21. Applicant: Medlogic Global Limited. Device class: 1.

Clearance details

Applicant: Medlogic Global Limited
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2003-04-25
Decision date: 2004-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plympton, Plymouth, Devon, GB

Download summary PDF View on FDA.gov ↗

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