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FDA 510(k)

3-WAY STOPCOCK

K-Number: K782168 · 1979-02-22

ApplicantMedex, Inc.
Decision Date1979-02-22
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

3-WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Medex, Inc.. It received FDA 510(k) clearance on 1979-02-22 under 510(k) number K782168. 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 3-WAY STOPCOCK?

3-WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1979-02-22. The listed applicant is Medex, Inc.. The 510(k) number is K782168.

When did 3-WAY STOPCOCK receive FDA 510(k) clearance?

3-WAY STOPCOCK received FDA 510(k) clearance on 1979-02-22, under 510(k) number K782168.

Who is the listed applicant for 3-WAY STOPCOCK?

The FDA 510(k) record lists Medex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3-WAY STOPCOCK?

The FDA product code for 3-WAY STOPCOCK is FMG.

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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.

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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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