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FDA 510(k)

SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH FILTER

K-Number: K113429 · 2012-03-12

Decision Date2012-03-12
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH 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 2012-03-12 under 510(k) number K113429. 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, AND SET WITH FILTER?

SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH FILTER is a medical device that received FDA 510(k) clearance on 2012-03-12. The listed applicant is Nipro Medical Corporation. The 510(k) number is K113429.

When did SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH FILTER receive FDA 510(k) clearance?

SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH FILTER received FDA 510(k) clearance on 2012-03-12, under 510(k) number K113429.

Who is the listed applicant for SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH 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, AND SET WITH FILTER?

The FDA product code for SAFETOUCH PSV WINGED INFUSION SET, AND SET WITH FILTER is FOZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Nipro Medical Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 33 devices →

Related Devices (Code: FOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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