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FDA 510(k)

JMS BYPASS TUBE

K-Number: K032977 · 2004-05-25

ApplicantJms North America Corp.
Decision Date2004-05-25
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JMS BYPASS TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Jms North America Corp.. It received FDA 510(k) clearance on 2004-05-25 under 510(k) number K032977. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JMS BYPASS TUBE?

JMS BYPASS TUBE is a medical device that received FDA 510(k) clearance on 2004-05-25. The listed applicant is Jms North America Corp.. The 510(k) number is K032977.

When did JMS BYPASS TUBE receive FDA 510(k) clearance?

JMS BYPASS TUBE received FDA 510(k) clearance on 2004-05-25, under 510(k) number K032977.

Who is the listed applicant for JMS BYPASS TUBE?

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 BYPASS TUBE?

The FDA product code for JMS BYPASS TUBE is DWF.

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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.

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Related Devices (Code: DWF)

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.

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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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