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FDA 510(k)

4 PORT, 4 WAY STOPCOCK

K-Number: K010217 · 2001-03-18

Decision Date2001-03-18
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

4 PORT, 4 WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is George Loo, MD. It received FDA 510(k) clearance on 2001-03-18 under 510(k) number K010217. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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