STOPCOCK 2-WAY, 3-WAY & 4-WAY
K-Number: K802258 · 1980-09-26
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Device Summary
Frequently Asked Questions
What is the STOPCOCK 2-WAY, 3-WAY & 4-WAY?
STOPCOCK 2-WAY, 3-WAY & 4-WAY is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Stanco Medical, Inc.. The 510(k) number is K802258.
When did STOPCOCK 2-WAY, 3-WAY & 4-WAY receive FDA 510(k) clearance?
STOPCOCK 2-WAY, 3-WAY & 4-WAY received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802258.
Who is the listed applicant for STOPCOCK 2-WAY, 3-WAY & 4-WAY?
The FDA 510(k) record lists Stanco Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOPCOCK 2-WAY, 3-WAY & 4-WAY?
The FDA product code for STOPCOCK 2-WAY, 3-WAY & 4-WAY 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 Stanco Medical, Inc. 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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