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FDA 510(k)

The Nanostim Introducer Kit

K-Number: K160716 · 2016-04-14

Decision Date2016-04-14
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

The Nanostim Introducer Kit is the device name listed in this FDA 510(k) record. The listed applicant is St. Jude Medical, Inc.. It received FDA 510(k) clearance on 2016-04-14 under 510(k) number K160716. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The Nanostim Introducer Kit?

The Nanostim Introducer Kit is a medical device that received FDA 510(k) clearance on 2016-04-14. The listed applicant is St. Jude Medical, Inc.. The 510(k) number is K160716.

When did The Nanostim Introducer Kit receive FDA 510(k) clearance?

The Nanostim Introducer Kit received FDA 510(k) clearance on 2016-04-14, under 510(k) number K160716.

Who is the listed applicant for The Nanostim Introducer Kit?

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

What is the FDA product code for The Nanostim Introducer Kit?

The FDA product code for The Nanostim Introducer Kit is DYB.

Other records listing St. Jude Medical, 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.

View all 19 devices →

Related Devices (Code: DYB)

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.