VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS
K-Number: K904886 · 1991-01-11
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Device Summary
Frequently Asked Questions
What is the VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS?
VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS is a medical device that received FDA 510(k) clearance on 1991-01-11. The listed applicant is Florida Infusion Services, Inc.. The 510(k) number is K904886.
When did VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS receive FDA 510(k) clearance?
VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS received FDA 510(k) clearance on 1991-01-11, under 510(k) number K904886.
Who is the listed applicant for VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS?
The FDA 510(k) record lists Florida Infusion Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS?
The FDA product code for VASCULAR ACCESS PORT CONTINUOUS INFUSION SETS is FPA.
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.
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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