Hospira Sapphire Sets— 510(k) K160492

Substantially Equivalent

Hospira, Inc.

FDA 510(k) clearance K160492 for Hospira Sapphire Sets, Substantially Equivalent on 2016-12-06. Applicant: Hospira, Inc.. Device class: 2.

Clearance details

Applicant: Hospira, Inc.
Product code: Code MRZ
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2016-02-22
Decision date: 2016-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, IL, 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.