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FDA 510(k)

VENNETO

K-Number: K974045 · 1997-11-20

ApplicantAmsure Sports, Inc.
Decision Date1997-11-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VENNETO is the device name listed in this FDA 510(k) record. The listed applicant is Amsure Sports, Inc.. It received FDA 510(k) clearance on 1997-11-20 under 510(k) number K974045. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENNETO?

VENNETO is a medical device that received FDA 510(k) clearance on 1997-11-20. The listed applicant is Amsure Sports, Inc.. The 510(k) number is K974045.

When did VENNETO receive FDA 510(k) clearance?

VENNETO received FDA 510(k) clearance on 1997-11-20, under 510(k) number K974045.

Who is the listed applicant for VENNETO?

The FDA 510(k) record lists Amsure Sports, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENNETO?

The FDA product code for VENNETO is HQY.

Related Clinical Trials

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Related Devices (Code: HQY)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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