INTRAVASCULAR CATHETER SET
K-Number: K830539 · 1983-03-17
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Device Summary
Frequently Asked Questions
What is the INTRAVASCULAR CATHETER SET?
INTRAVASCULAR CATHETER SET is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Lab-A-Cath Corp.. The 510(k) number is K830539.
When did INTRAVASCULAR CATHETER SET receive FDA 510(k) clearance?
INTRAVASCULAR CATHETER SET received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830539.
Who is the listed applicant for INTRAVASCULAR CATHETER SET?
The FDA 510(k) record lists Lab-A-Cath Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAVASCULAR CATHETER SET?
The FDA product code for INTRAVASCULAR CATHETER SET is FOZ.
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: FOZ)
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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