4 PORT, 4 WAY STOPCOCK
K-Number: K010217 · 2001-03-18
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Device Summary
Frequently Asked Questions
What is the 4 PORT, 4 WAY STOPCOCK?
4 PORT, 4 WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 2001-03-18. The listed applicant is George Loo, MD. The 510(k) number is K010217.
When did 4 PORT, 4 WAY STOPCOCK receive FDA 510(k) clearance?
4 PORT, 4 WAY STOPCOCK received FDA 510(k) clearance on 2001-03-18, under 510(k) number K010217.
Who is the listed applicant for 4 PORT, 4 WAY STOPCOCK?
The FDA 510(k) record lists George Loo, MD as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 4 PORT, 4 WAY STOPCOCK?
The FDA product code for 4 PORT, 4 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.
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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