LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020— 510(k) K023163

Name: FDA 510(k) clearance K023163
Creator: U.S. Food and Drug Administration
Published: 2003-01-13

Substantially Equivalent

Medlogic Global Limited

FDA 510(k) clearance K023163 for LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020, Substantially Equivalent on 2003-01-13. 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: 2002-09-23
Decision date: 2003-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plympton, Plymouth, Devon, GB

Download summary PDF View on FDA.gov ↗

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