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FDA 510(k)

HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM

K-Number: K090610 · 2009-03-13

ApplicantHospira, Inc.
Decision Date2009-03-13
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2009-03-13 under 510(k) number K090610. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM?

HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2009-03-13. The listed applicant is Hospira, Inc.. The 510(k) number is K090610.

When did HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM receive FDA 510(k) clearance?

HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM received FDA 510(k) clearance on 2009-03-13, under 510(k) number K090610.

Who is the listed applicant for HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM?

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 HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM?

The FDA product code for HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM is DRG.

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Other records listing Hospira, Inc. as applicant

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Official Source

View on FDA Database →

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

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