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FDA 510(k)

VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM

K-Number: K935778 · 1996-12-05

Decision Date1996-12-05
Product CodeCCE
Advisory CommitteeAN
DecisionUnknown

Device Summary

VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Via Medical Corp.. It received FDA 510(k) clearance on 1996-12-05 under 510(k) number K935778. The device is classified under product code CCE. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM?

VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-12-05. The listed applicant is Via Medical Corp.. The 510(k) number is K935778.

When did VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM receive FDA 510(k) clearance?

VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM received FDA 510(k) clearance on 1996-12-05, under 510(k) number K935778.

Who is the listed applicant for VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM?

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

What is the FDA product code for VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM?

The FDA product code for VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEM is CCE.

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 Via Medical Corp. 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.

Related Devices (Code: CCE)

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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