STOPCOCK
K-Number: K780596 · 1978-04-19
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Device Summary
Frequently Asked Questions
What is the STOPCOCK?
STOPCOCK is a medical device that received FDA 510(k) clearance on 1978-04-19. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K780596.
When did STOPCOCK receive FDA 510(k) clearance?
STOPCOCK received FDA 510(k) clearance on 1978-04-19, under 510(k) number K780596.
Who is the listed applicant for STOPCOCK?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOPCOCK?
The FDA product code for 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 Abco Dealers, 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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