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FDA 510(k)

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL

K-Number: K925228 · 1993-07-30

ApplicantY
Decision Date1993-07-30
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL is the device name listed in this FDA 510(k) record. The listed applicant is Y. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K925228. 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 IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL?

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Y. The 510(k) number is K925228.

When did IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL receive FDA 510(k) clearance?

IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL received FDA 510(k) clearance on 1993-07-30, under 510(k) number K925228.

Who is the listed applicant for IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL?

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

What is the FDA product code for IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL?

The FDA product code for IVAC 59 SERIES UNIVERSAL SET W/ ANTI-FREE FLOW VAL 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 Y 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.

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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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