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FDA 510(k)

MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM

K-Number: K070475 · 2007-05-07

Decision Date2007-05-07
Product CodeNEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING 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 2007-05-07 under 510(k) number K070475. The device is classified under product code NEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM?

MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2007-05-07. The listed applicant is Given Imaging , Ltd.. The 510(k) number is K070475.

When did MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM receive FDA 510(k) clearance?

MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM received FDA 510(k) clearance on 2007-05-07, under 510(k) number K070475.

Who is the listed applicant for MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING 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 MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM?

The FDA product code for MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM is NEZ.

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.

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Related Devices (Code: NEZ)

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

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