CRITERION, CRITERION I.V., MODIFIED
K-Number: K952267 · 1997-12-02
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Device Summary
Frequently Asked Questions
What is the CRITERION, CRITERION I.V., MODIFIED?
CRITERION, CRITERION I.V., MODIFIED is a medical device that received FDA 510(k) clearance on 1997-12-02. The listed applicant is Nova-Ventrx. The 510(k) number is K952267.
When did CRITERION, CRITERION I.V., MODIFIED receive FDA 510(k) clearance?
CRITERION, CRITERION I.V., MODIFIED received FDA 510(k) clearance on 1997-12-02, under 510(k) number K952267.
Who is the listed applicant for CRITERION, CRITERION I.V., MODIFIED?
The FDA 510(k) record lists Nova-Ventrx as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRITERION, CRITERION I.V., MODIFIED?
The FDA product code for CRITERION, CRITERION I.V., MODIFIED is BZE.
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 Nova-Ventrx 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: BZE)
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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