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FDA 510(k)

Senhance Surgical System

K-Number: K220889 · 2022-05-27

Decision Date2022-05-27
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Senhance Surgical System is the device name listed in this FDA 510(k) record. The listed applicant is Asensus Surgical, Inc.. It received FDA 510(k) clearance on 2022-05-27 under 510(k) number K220889. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Senhance Surgical System?

Senhance Surgical System is a medical device that received FDA 510(k) clearance on 2022-05-27. The listed applicant is Asensus Surgical, Inc.. The 510(k) number is K220889.

When did Senhance Surgical System receive FDA 510(k) clearance?

Senhance Surgical System received FDA 510(k) clearance on 2022-05-27, under 510(k) number K220889.

Who is the listed applicant for Senhance Surgical System?

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

What is the FDA product code for Senhance Surgical System?

The FDA product code for Senhance Surgical System is NAY.

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 Asensus Surgical, 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: NAY)

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

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