JMS PLANECTA STOPCOCK
K-Number: K070143 · 2007-04-10
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Device Summary
Frequently Asked Questions
What is the JMS PLANECTA STOPCOCK?
JMS PLANECTA STOPCOCK is a medical device that received FDA 510(k) clearance on 2007-04-10. The listed applicant is Jms North America Corp.. The 510(k) number is K070143.
When did JMS PLANECTA STOPCOCK receive FDA 510(k) clearance?
JMS PLANECTA STOPCOCK received FDA 510(k) clearance on 2007-04-10, under 510(k) number K070143.
Who is the listed applicant for JMS PLANECTA STOPCOCK?
The FDA 510(k) record lists Jms North America Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JMS PLANECTA STOPCOCK?
The FDA product code for JMS PLANECTA 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 Jms North America Corp. 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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