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FDA 510(k)

EXEL THREE-WAY STOPCOCK

K-Number: K862492 · 1986-09-25

ApplicantExel Intl.
Decision Date1986-09-25
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXEL THREE-WAY STOPCOCK is the device name listed in this FDA 510(k) record. The listed applicant is Exel Intl.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K862492. 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 EXEL THREE-WAY STOPCOCK?

EXEL THREE-WAY STOPCOCK is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is Exel Intl.. The 510(k) number is K862492.

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

EXEL THREE-WAY STOPCOCK received FDA 510(k) clearance on 1986-09-25, under 510(k) number K862492.

Who is the listed applicant for EXEL THREE-WAY STOPCOCK?

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

What is the FDA product code for EXEL THREE-WAY STOPCOCK?

The FDA product code for EXEL 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 Exel Intl. 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.

View all 18 devices →

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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