KY Banksy Aloe
K-Number: K183302 · 2019-04-16
ApplicantRb Health (Us), LLC
Decision Date2019-04-16
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
KY Banksy Aloe is a medical device manufactured by Rb Health (Us), LLC. It received FDA 510(k) clearance on 2019-04-16 under approval number K183302. 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 Banksy Aloe?
KY Banksy Aloe is a medical device that received FDA 510(k) clearance on 2019-04-16. It is manufactured by Rb Health (Us), LLC. The 510(k) number is K183302.
When was KY Banksy Aloe approved by the FDA?
KY Banksy Aloe received FDA 510(k) clearance on 2019-04-16, under approval number K183302.
What company makes KY Banksy Aloe?
KY Banksy Aloe is manufactured by Rb Health (Us), LLC.
What is the FDA product code for KY Banksy Aloe?
The FDA product code for KY Banksy Aloe is NUC.
Other Devices by Rb Health (Us), LLC
Related Devices (Code: NUC)
K161585Mano and Mano Personal LubricantMano and Mano Proprietary Limited
K161544Trojan Chain Reaction Personal LubricantChurch & Dwight Co., Inc.
K161385Just Like Me Personal LubricantWtfn-Dba Classic Erotica/Holiday Products
K152671Pulse Aloe-ahhToaster Labs, Inc.
K152628Pulse H20h!Toaster Labs, Inc.
K153372Repagyn vaginal suppositoriesFarma-Derma S.R.L.
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.