PEDI-SPIDER STRAP— 510(k) K061721

Name: FDA 510(k) clearance K061721
Creator: U.S. Food and Drug Administration
Published: 2006-08-17

Substantially Equivalent

Emergency Products and Research

FDA 510(k) clearance K061721 for PEDI-SPIDER STRAP, Substantially Equivalent on 2006-08-17. Applicant: Emergency Products and Research. Device class: 1.

Clearance details

Applicant: Emergency Products and Research
Product code: Code NZD
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 2006-06-19
Decision date: 2006-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kent, OH, US

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