KY Grosz Liquid
K-Number: K193032 · 2020-04-20
ApplicantRb Health (Us), LLC
Decision Date2020-04-20
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
KY Grosz Liquid is a medical device manufactured by Rb Health (Us), LLC. It received FDA 510(k) clearance on 2020-04-20 under approval number K193032. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the KY Grosz Liquid?
KY Grosz Liquid is a medical device that received FDA 510(k) clearance on 2020-04-20. It is manufactured by Rb Health (Us), LLC. The 510(k) number is K193032.
When was KY Grosz Liquid approved by the FDA?
KY Grosz Liquid received FDA 510(k) clearance on 2020-04-20, under approval number K193032.
What company makes KY Grosz Liquid?
KY Grosz Liquid is manufactured by Rb Health (Us), LLC.
What is the FDA product code for KY Grosz Liquid?
The FDA product code for KY Grosz Liquid is NUC.
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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.