Cleared Traditional

K112110 - STERILE LUBRICATING JELLY

K112110 is an FDA 510(k) clearance for STERILE LUBRICATING JELLY, manufactured by Jianerkang Medical Dressing Company. The device is a Class 1 General Hospital device with product code KMJ cleared through the Traditional 510(k) pathway after a 263-day FDA review.

K112110 · Jianerkang Medical Dressing Company · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Apr 2012
Decision
263d
Days
Class 1
Risk

K112110 is an FDA 510(k) clearance for the STERILE LUBRICATING JELLY. Classified as Lubricant, Patient (product code KMJ), Class I - General Controls.

Submitted by Jianerkang Medical Dressing Company (Jintan City, Jiangsu, CN). The FDA issued a Cleared decision on April 10, 2012 after a review of 263 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6375 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K112110

510(k) Number K112110 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 22, 2011
Decision Date April 10, 2012
Days to Decision 263 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
134d slower than avg
Panel avg: 129d · This submission: 263d
Pathway characteristics
Predicate-based equivalence.

KMJ Device Classification - Class 1, General Controls

Product Code KMJ Lubricant, Patient
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6375
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KMJ Lubricant, Patient

All 40
Devices cleared under the same product code (KMJ) and FDA review panel - the closest regulatory comparables to K112110.
COLONGLIDE(R) LUBRICANT
K131617 · Pediatric Pharmaceuticals, Inc. · Oct 2013
LUBE JELLY SURINGE
K121390 · Nurse Assist, Inc. · Aug 2012
DUKAL LUBRICATING JELLY
K113689 · Dukal Corporation · May 2012
DYNACOR LUBRICATION GEL
K103718 · Medline Industries, Inc. · May 2011
ULTRA SEAL STERILE LUBRICATING JELLY
K101522 · Ultra Seal Corporation · Dec 2010
DYNAREX STERILE LUBRICATING JELLY
K092488 · Dynarex Corporation · Dec 2009
K112110 · STERILE LUBRICATING JELLY
Download PDF FDA Summary Jianerkang Medical Dr…