FDA 510(k)

LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS

K-Number: K052722 · 2005-11-02

Decision Date2005-11-02

Product CodeFPA

Advisory CommitteeHO

DecisionUnknown

Device Summary

LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2005-11-02 under 510(k) number K052722. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS?

LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS is a medical device that received FDA 510(k) clearance on 2005-11-02. The listed applicant is Hospira, Inc.. The 510(k) number is K052722.

When did LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS receive FDA 510(k) clearance?

LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS received FDA 510(k) clearance on 2005-11-02, under 510(k) number K052722.

Who is the listed applicant for LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS?

The FDA 510(k) record lists Hospira, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS?

The FDA product code for LIFESHIELD LATEX-FREE MICROBORE EXTENSION SET, MODEL 14949 AND OTHERS is FPA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.