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FDA 510(k)

MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM

K-Number: K060805 · 2006-05-24

Decision Date2006-05-24
Product CodeNSI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Given Imaging , Ltd.. It received FDA 510(k) clearance on 2006-05-24 under 510(k) number K060805. The device is classified under product code NSI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM?

MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM is a medical device that received FDA 510(k) clearance on 2006-05-24. The listed applicant is Given Imaging , Ltd.. The 510(k) number is K060805.

When did MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM received FDA 510(k) clearance on 2006-05-24, under 510(k) number K060805.

Who is the listed applicant for MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM?

The FDA 510(k) record lists Given Imaging , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM?

The FDA product code for MODIFICATION TO GIVEN DIAGNOSTIC SYSTEM is NSI.

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 Given Imaging , Ltd. 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 27 devices →

Related Devices (Code: NSI)

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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