VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD.
K-Number: K922997 · 1994-01-11
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Device Summary
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
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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