Nuvis Battery Arthroscope
K-Number: K191594 · 2019-07-11
ApplicantIntegrated Endoscopy, Inc.
Decision Date2019-07-11
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Nuvis Battery Arthroscope is a medical device manufactured by Integrated Endoscopy, Inc.. It received FDA 510(k) clearance on 2019-07-11 under approval number K191594. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nuvis Battery Arthroscope?
Nuvis Battery Arthroscope is a medical device that received FDA 510(k) clearance on 2019-07-11. It is manufactured by Integrated Endoscopy, Inc.. The 510(k) number is K191594.
When was Nuvis Battery Arthroscope approved by the FDA?
Nuvis Battery Arthroscope received FDA 510(k) clearance on 2019-07-11, under approval number K191594.
What company makes Nuvis Battery Arthroscope?
Nuvis Battery Arthroscope is manufactured by Integrated Endoscopy, Inc..
What is the FDA product code for Nuvis Battery Arthroscope?
The FDA product code for Nuvis Battery Arthroscope is HRX.
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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.