ARTERIAL EXTENSION SET
K-Number: K850088 · 1985-02-02
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Device Summary
Frequently Asked Questions
What is the ARTERIAL EXTENSION SET?
ARTERIAL EXTENSION SET is a medical device that received FDA 510(k) clearance on 1985-02-02. The listed applicant is Medical Matrix, Inc.. The 510(k) number is K850088.
When did ARTERIAL EXTENSION SET receive FDA 510(k) clearance?
ARTERIAL EXTENSION SET received FDA 510(k) clearance on 1985-02-02, under 510(k) number K850088.
Who is the listed applicant for ARTERIAL EXTENSION SET?
The FDA 510(k) record lists Medical Matrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTERIAL EXTENSION SET?
The FDA product code for ARTERIAL EXTENSION 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 Medical Matrix, 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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