VASCULAR ACCESS PORT CONTINUOUS INFUSION SET
K-Number: K891226 · 1989-05-30
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Device Summary
Frequently Asked Questions
What is the VASCULAR ACCESS PORT CONTINUOUS INFUSION SET?
VASCULAR ACCESS PORT CONTINUOUS INFUSION SET is a medical device that received FDA 510(k) clearance on 1989-05-30. The listed applicant is Infucare Products, Inc.. The 510(k) number is K891226.
When did VASCULAR ACCESS PORT CONTINUOUS INFUSION SET receive FDA 510(k) clearance?
VASCULAR ACCESS PORT CONTINUOUS INFUSION SET received FDA 510(k) clearance on 1989-05-30, under 510(k) number K891226.
Who is the listed applicant for VASCULAR ACCESS PORT CONTINUOUS INFUSION SET?
The FDA 510(k) record lists Infucare Products, 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 SET?
The FDA product code for VASCULAR ACCESS PORT CONTINUOUS INFUSION SET 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.
Other records listing Infucare Products, Inc. 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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