RP Lite 760R
K-Number: K163280 · 2017-01-27
ApplicantMego Afek AC , Ltd.
Decision Date2017-01-27
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
RP Lite 760R is a medical device manufactured by Mego Afek AC , Ltd.. It received FDA 510(k) clearance on 2017-01-27 under approval number K163280. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the RP Lite 760R?
RP Lite 760R is a medical device that received FDA 510(k) clearance on 2017-01-27. It is manufactured by Mego Afek AC , Ltd.. The 510(k) number is K163280.
When was RP Lite 760R approved by the FDA?
RP Lite 760R received FDA 510(k) clearance on 2017-01-27, under approval number K163280.
What company makes RP Lite 760R?
RP Lite 760R is manufactured by Mego Afek AC , Ltd..
What is the FDA product code for RP Lite 760R?
The FDA product code for RP Lite 760R is IRP.
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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.