HMP DUAL POLYSULFONE PORT
K-Number: K934640 · 1994-02-25
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Device Summary
Frequently Asked Questions
What is the HMP DUAL POLYSULFONE PORT?
HMP DUAL POLYSULFONE PORT is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Horizon Medical Products, Inc.. The 510(k) number is K934640.
When did HMP DUAL POLYSULFONE PORT receive FDA 510(k) clearance?
HMP DUAL POLYSULFONE PORT received FDA 510(k) clearance on 1994-02-25, under 510(k) number K934640.
Who is the listed applicant for HMP DUAL POLYSULFONE PORT?
The FDA 510(k) record lists Horizon Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HMP DUAL POLYSULFONE PORT?
The FDA product code for HMP DUAL POLYSULFONE 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 Horizon Medical 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: 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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