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FDA 510(k)

VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.

K-Number: K922997 · 1994-01-11

Decision Date1994-01-11
Product CodeLZF
Advisory CommitteeHO
DecisionUnknown

Device Summary

VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. 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 1994-01-11 under 510(k) number K922997. The device is classified under product code LZF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.?

VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is Via Medical Corp.. The 510(k) number is K922997.

When did VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. receive FDA 510(k) clearance?

VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. received FDA 510(k) clearance on 1994-01-11, under 510(k) number K922997.

Who is the listed applicant for VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.?

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 CHEM. SYST. -- MOD.?

The FDA product code for VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. is LZF.

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: LZF)

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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