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FDA 510(k)

SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER

K-Number: K132153 · 2013-12-05

ApplicantNipro Medical Corporation
Decision Date2013-12-05
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corporation. It received FDA 510(k) clearance on 2013-12-05 under 510(k) number K132153. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER?

SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER is a medical device that received FDA 510(k) clearance on 2013-12-05. The listed applicant is Nipro Medical Corporation. The 510(k) number is K132153.

When did SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER receive FDA 510(k) clearance?

SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER received FDA 510(k) clearance on 2013-12-05, under 510(k) number K132153.

Who is the listed applicant for SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER?

The FDA 510(k) record lists Nipro Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER?

The FDA product code for SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER is FOZ.

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Other records listing Nipro Medical Corporation as applicant

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Related Devices (Code: FOZ)

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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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