K-Y BRAND ULTRA GEL PERSONAL LUBRICANT

Lubricant, Personal

PERSONAL PRODUCTS CO., DIV. OF MCNEIL PPC, INC.

The following data is part of a premarket notification filed by Personal Products Co., Div. Of Mcneil Ppc, Inc. with the FDA for K-y Brand Ultra Gel Personal Lubricant.

Pre-market Notification Details

Device IDK020827
510k NumberK020827
Device Name:K-Y BRAND ULTRA GEL PERSONAL LUBRICANT
ClassificationLubricant, Personal
Applicant PERSONAL PRODUCTS CO., DIV. OF MCNEIL PPC, INC. 199 GRANDVIEW RD. Skillman,  NJ  08558 -9418
ContactMarylou Panico
CorrespondentMarylou Panico
PERSONAL PRODUCTS CO., DIV. OF MCNEIL PPC, INC. 199 GRANDVIEW RD. Skillman,  NJ  08558 -9418
Product CodeNUC  
CFR Regulation Number884.5300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-03-14
Decision Date2002-06-12
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10067981087373 K020827 000
10067981087359 K020827 000

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