Medley
K-Number: K212000 · 2021-11-18
ApplicantGood Clean Love, Inc.
Decision Date2021-11-18
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Medley is a medical device manufactured by Good Clean Love, Inc.. It received FDA 510(k) clearance on 2021-11-18 under approval number K212000. 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 Medley?
Medley is a medical device that received FDA 510(k) clearance on 2021-11-18. It is manufactured by Good Clean Love, Inc.. The 510(k) number is K212000.
When was Medley approved by the FDA?
Medley received FDA 510(k) clearance on 2021-11-18, under approval number K212000.
What company makes Medley?
Medley is manufactured by Good Clean Love, Inc..
What is the FDA product code for Medley?
The FDA product code for Medley is NUC.
Other Devices by Good Clean Love, Inc.
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.