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FDA 510(k)

K-Y LUBRICATING JELLY

K-Number: K810310 · 1981-04-21

Decision Date1981-04-21
Product CodeKMJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

K-Y LUBRICATING JELLY is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1981-04-21 under 510(k) number K810310. The device is classified under product code KMJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-Y LUBRICATING JELLY?

K-Y LUBRICATING JELLY is a medical device that received FDA 510(k) clearance on 1981-04-21. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K810310.

When did K-Y LUBRICATING JELLY receive FDA 510(k) clearance?

K-Y LUBRICATING JELLY received FDA 510(k) clearance on 1981-04-21, under 510(k) number K810310.

Who is the listed applicant for K-Y LUBRICATING JELLY?

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

What is the FDA product code for K-Y LUBRICATING JELLY?

The FDA product code for K-Y LUBRICATING JELLY is KMJ.

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 Johnson & Johnson Professionals, Inc. 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 206 devices →

Related Devices (Code: KMJ)

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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