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FDA 510(k)

PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE

K-Number: K101200 · 2010-09-30

Decision Date2010-09-30
Product CodeNEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE 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 2010-09-30 under 510(k) number K101200. 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 PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE?

PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE is a medical device that received FDA 510(k) clearance on 2010-09-30. The listed applicant is Given Imaging , Ltd.. The 510(k) number is K101200.

When did PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE receive FDA 510(k) clearance?

PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE received FDA 510(k) clearance on 2010-09-30, under 510(k) number K101200.

Who is the listed applicant for PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE?

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 PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE?

The FDA product code for PILLCAM EXPRESS VIDEO CAPSULES DELIVERY DEVICE 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.

View all 27 devices →

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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