VYGON NEO-SUMP
K-Number: K974806 · 1998-03-23
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Device Summary
Frequently Asked Questions
What is the VYGON NEO-SUMP?
VYGON NEO-SUMP is a medical device that received FDA 510(k) clearance on 1998-03-23. The listed applicant is Vygon Corp.. The 510(k) number is K974806.
When did VYGON NEO-SUMP receive FDA 510(k) clearance?
VYGON NEO-SUMP received FDA 510(k) clearance on 1998-03-23, under 510(k) number K974806.
Who is the listed applicant for VYGON NEO-SUMP?
The FDA 510(k) record lists Vygon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VYGON NEO-SUMP?
The FDA product code for VYGON NEO-SUMP is KNT.
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 Vygon 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: KNT)
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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