RAPID Web
K-Number: K170839 · 2017-05-26
ApplicantGiven Imaging , Ltd.
Decision Date2017-05-26
Product CodeNEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
RAPID Web is a medical device manufactured by Given Imaging , Ltd.. It received FDA 510(k) clearance on 2017-05-26 under approval number K170839. 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 RAPID Web?
RAPID Web is a medical device that received FDA 510(k) clearance on 2017-05-26. It is manufactured by Given Imaging , Ltd.. The 510(k) number is K170839.
When was RAPID Web approved by the FDA?
RAPID Web received FDA 510(k) clearance on 2017-05-26, under approval number K170839.
What company makes RAPID Web?
RAPID Web is manufactured by Given Imaging , Ltd..
What is the FDA product code for RAPID Web?
The FDA product code for RAPID Web is NEZ.
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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.