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FDA 510(k)

K-Y BRAND LIQUIBEADS

K-Number: K122061 · 2013-11-08

Decision Date2013-11-08
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

K-Y BRAND LIQUIBEADS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Healthcare Products. It received FDA 510(k) clearance on 2013-11-08 under 510(k) number K122061. 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 K-Y BRAND LIQUIBEADS?

K-Y BRAND LIQUIBEADS is a medical device that received FDA 510(k) clearance on 2013-11-08. The listed applicant is Johnson & Johnson Healthcare Products. The 510(k) number is K122061.

When did K-Y BRAND LIQUIBEADS receive FDA 510(k) clearance?

K-Y BRAND LIQUIBEADS received FDA 510(k) clearance on 2013-11-08, under 510(k) number K122061.

Who is the listed applicant for K-Y BRAND LIQUIBEADS?

The FDA 510(k) record lists Johnson & Johnson Healthcare Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K-Y BRAND LIQUIBEADS?

The FDA product code for K-Y BRAND LIQUIBEADS is NUC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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