Today Personal Lubricant

FDA 510(k) K851617 · Vli Corp.

Substantially Equivalent

510(k) numberK851617

Submission

Device name
Today Personal Lubricant
Applicant
Vli Corp.
Washington, DC, US
Received
April 18, 1985
Decision date
June 6, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KMJ – Lubricant, Patient
Device class
Class I (low risk)
Regulation
21 CFR 880.6375
Specialty
General Hospital

Other 510(k)s with product code KMJ

510(k)DeviceApplicantDecision
K142473Lubricating JellyKMJ · Traditional Sion Biotext Medical , Ltd.04/13/2015SE
K141028Colonglide LubricantKMJ · Special Pediatric Pharmaceuticals, Inc.07/24/2014SE
K131617Colonglide(R) LubricantKMJ · Traditional Pediatric Pharmaceuticals, Inc.10/03/2013SE
K121390Lube Jelly SuringeKMJ · Traditional Nurse Assist, Inc.08/10/2012SE
K113689Dukal Lubricating JellyKMJ · Traditional Dukal Corporation05/04/2012SE
K112110Sterile Lubricating JellyKMJ · Traditional Jianerkang Medical Dressing Company04/10/2012SE
K103718Dynacor Lubrication GelKMJ · Traditional Medline Industries, Inc.05/10/2011SE
K101522Ultra Seal Sterile Lubricating JellyKMJ · Traditional Ultra Seal Corporation12/23/2010SE
K092488Dynarex Sterile Lubricating JellyKMJ · Traditional Dynarex Corporation12/18/2009SE
K083189Steri-Lub Lubrication GelKMJ · Special Avail Medical Products, Inc.11/21/2008SE

Questions and answers

When was Today Personal Lubricant cleared by the FDA?

Today Personal Lubricant (K851617) received a 510(k) decision of Substantially Equivalent on June 6, 1985, 49 days after the submission was received.

What is the product code of K851617?

The FDA product code is KMJ – Lubricant, Patient, a Class I (low risk) device regulated under 21 CFR 880.6375.