K-number	K211152
Device name	Durex Condom with Benzocaine
Applicant	Rb Health (Us), LLC
Product code	HIS
Device class	Class II
Decision date	May 11, 2022
Decision	Substantially Equivalent
Regulation	884.5300

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Source

View the full FDA submission: accessdata.fda.gov

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Durex Condom with Benzocaine

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