TERUFUSION THREE-WAY STOPCOCK
K-Number: K823469 · 1982-12-30
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Device Summary
Frequently Asked Questions
What is the TERUFUSION THREE-WAY STOPCOCK?
TERUFUSION THREE-WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Terumo Medical Corp.. The 510(k) number is K823469.
When did TERUFUSION THREE-WAY STOPCOCK receive FDA 510(k) clearance?
TERUFUSION THREE-WAY STOPCOCK received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823469.
Who is the listed applicant for TERUFUSION THREE-WAY STOPCOCK?
The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TERUFUSION THREE-WAY STOPCOCK?
The FDA product code for TERUFUSION THREE-WAY STOPCOCK is FMG.
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 Terumo Medical 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: FMG)
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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