K-Y Marilyn Pleasure Gel— 510(k) K151884

Name: FDA 510(k) clearance K151884
Creator: U.S. Food and Drug Administration
Published: 2016-01-11

Substantially Equivalent

Reckitt Benckiser, LLC

FDA 510(k) clearance K151884 for K-Y Marilyn Pleasure Gel, Substantially Equivalent on 2016-01-11. Applicant: Reckitt Benckiser, LLC. Device class: 2.

Clearance details

Applicant: Reckitt Benckiser, LLC
Product code: Code NUC
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 2015-07-09
Decision date: 2016-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Parsippany, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NUC

product code NUC

Other: 8
Total: 8

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.