Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

K-Y BRAND WARMING LIQUID

K-Number: K070545 · 2007-03-23

Decision Date2007-03-23
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

K-Y BRAND WARMING LIQUID is the device name listed in this FDA 510(k) record. The listed applicant is Personal Products Co.. It received FDA 510(k) clearance on 2007-03-23 under 510(k) number K070545. 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 WARMING LIQUID?

K-Y BRAND WARMING LIQUID is a medical device that received FDA 510(k) clearance on 2007-03-23. The listed applicant is Personal Products Co.. The 510(k) number is K070545.

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

K-Y BRAND WARMING LIQUID received FDA 510(k) clearance on 2007-03-23, under 510(k) number K070545.

Who is the listed applicant for K-Y BRAND WARMING LIQUID?

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

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

The FDA product code for K-Y BRAND WARMING LIQUID 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.

Other records listing Personal Products Co. as applicant

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.

View all 45 devices →

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

View on FDA Database →

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

↑