EXEL THREE-WAY STOPCOCK
K-Number: K862492 · 1986-09-25
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Device Summary
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.
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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