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FDA 510(k)

OSBON PERSONAL LUBRICANT

K-Number: K895406 · 1989-12-01

ApplicantOsbon Medical Systems, Ltd.
Decision Date1989-12-01
Product CodeKMJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OSBON PERSONAL LUBRICANT is the device name listed in this FDA 510(k) record. The listed applicant is Osbon Medical Systems, Ltd.. It received FDA 510(k) clearance on 1989-12-01 under 510(k) number K895406. 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 OSBON PERSONAL LUBRICANT?

OSBON PERSONAL LUBRICANT is a medical device that received FDA 510(k) clearance on 1989-12-01. The listed applicant is Osbon Medical Systems, Ltd.. The 510(k) number is K895406.

When did OSBON PERSONAL LUBRICANT receive FDA 510(k) clearance?

OSBON PERSONAL LUBRICANT received FDA 510(k) clearance on 1989-12-01, under 510(k) number K895406.

Who is the listed applicant for OSBON PERSONAL LUBRICANT?

The FDA 510(k) record lists Osbon Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSBON PERSONAL LUBRICANT?

The FDA product code for OSBON PERSONAL LUBRICANT 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Osbon Medical Systems, Ltd. 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.

K912736ERECAID(R) SYSTEM PLUSK901318STAYEREC SYSTEM(TM)K896207OSBON PERSONAL LUBRICANT

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.

K131617COLONGLIDE(R) LUBRICANTPediatric Pharmaceuticals, Inc.K121390LUBE JELLY SURINGENurse Assist, Inc.K113689DUKAL LUBRICATING JELLYDukal CorporationK112110STERILE LUBRICATING JELLYJianerkang Medical Dressing CompanyK103718DYNACOR LUBRICATION GELMedline Industries, Inc.K101522ULTRA SEAL STERILE LUBRICATING JELLYUltra Seal Corporation

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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