ROBIN HOOD VEST— 510(k) K051300

Substantially Equivalent

Kamber Corporation

FDA 510(k) clearance K051300 for ROBIN HOOD VEST, Substantially Equivalent on 2005-12-08. Applicant: Kamber Corporation. Device class: 1.

Clearance details

Applicant: Kamber Corporation
Product code: Code FRP
Device class: Class 1
Regulation: 21 CFR 880.5680
Advisory panel: General Hospital
Date received: 2005-05-18
Decision date: 2005-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.