FLU VEN I.V. SETS
K-Number: K811914 · 1981-08-03
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Device Summary
Frequently Asked Questions
What is the FLU VEN I.V. SETS?
FLU VEN I.V. SETS is a medical device that received FDA 510(k) clearance on 1981-08-03. The listed applicant is Venusa , Ltd.. The 510(k) number is K811914.
When did FLU VEN I.V. SETS receive FDA 510(k) clearance?
FLU VEN I.V. SETS received FDA 510(k) clearance on 1981-08-03, under 510(k) number K811914.
Who is the listed applicant for FLU VEN I.V. SETS?
The FDA 510(k) record lists Venusa , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLU VEN I.V. SETS?
The FDA product code for FLU VEN I.V. SETS is FPA.
Other records listing Venusa , Ltd. 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: 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
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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