INFUSAID INFUSE-A-PORT
K-Number: K842355 · 1984-08-06
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Device Summary
Frequently Asked Questions
What is the INFUSAID INFUSE-A-PORT?
INFUSAID INFUSE-A-PORT is a medical device that received FDA 510(k) clearance on 1984-08-06. The listed applicant is Infusaid Corp.. The 510(k) number is K842355.
When did INFUSAID INFUSE-A-PORT receive FDA 510(k) clearance?
INFUSAID INFUSE-A-PORT received FDA 510(k) clearance on 1984-08-06, under 510(k) number K842355.
Who is the listed applicant for INFUSAID INFUSE-A-PORT?
The FDA 510(k) record lists Infusaid Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSAID INFUSE-A-PORT?
The FDA product code for INFUSAID INFUSE-A-PORT is LJT.
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 Infusaid 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: LJT)
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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