MODIFICATON TO: GIVEN DIAGNOSTIC IMAGING SYSTEM
K-Number: K070475 · 2007-05-07
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Device Summary
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.
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
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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