READI-STRAND, MODEL PSSTRAND— 510(k) K023179

Name: FDA 510(k) clearance K023179
Creator: U.S. Food and Drug Administration
Published: 2003-07-02

Substantially Equivalent

Worldwide Medical Technologies, LLC

FDA 510(k) clearance K023179 for READI-STRAND, MODEL PSSTRAND, Substantially Equivalent on 2003-07-02. Applicant: Worldwide Medical Technologies, LLC. Device class: 2.

Clearance details

Applicant: Worldwide Medical Technologies, LLC
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 2002-09-24
Decision date: 2003-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodbury, CT, US

Download summary PDF View on FDA.gov ↗

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