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FDA 510(k)

SYLK PERSONAL LUBRICANT

K-Number: K152646 · 2016-03-11

ApplicantToro Management, LLC Dba Sylk
Decision Date2016-03-11
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SYLK PERSONAL LUBRICANT is a medical device manufactured by Toro Management, LLC Dba Sylk. It received FDA 510(k) clearance on 2016-03-11 under approval number K152646. 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 SYLK PERSONAL LUBRICANT?

SYLK PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 2016-03-11. It is manufactured by Toro Management, LLC Dba Sylk. The 510(k) number is K152646.

When was SYLK PERSONAL LUBRICANT approved by the FDA?

SYLK PERSONAL LUBRICANT received FDA 510(k) clearance on 2016-03-11, under approval number K152646.

What company makes SYLK PERSONAL LUBRICANT?

SYLK PERSONAL LUBRICANT is manufactured by Toro Management, LLC Dba Sylk.

What is the FDA product code for SYLK PERSONAL LUBRICANT?

The FDA product code for SYLK PERSONAL LUBRICANT is NUC.

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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.

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