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FDA 510(k)

WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM

K-Number: K940056 · 1994-04-04

Decision Date1994-04-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Puritas Health Care, Inc.. It received FDA 510(k) clearance on 1994-04-04 under 510(k) number K940056. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM?

WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM is a medical device that received FDA 510(k) clearance on 1994-04-04. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K940056.

When did WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM receive FDA 510(k) clearance?

WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM received FDA 510(k) clearance on 1994-04-04, under 510(k) number K940056.

Who is the listed applicant for WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM?

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

What is the FDA product code for WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM?

The FDA product code for WINGED INFUSION SET A-PORT VASCULAR ACCESS SYSTEM is FPA.

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 Puritas Health Care, Inc. 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 24 devices →

Related Devices (Code: FPA)

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

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

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