LUBRICATING JELLY— 510(k) K903910

Substantially Equivalent

Lake Pharmaceutical, Inc.

FDA 510(k) clearance K903910 for LUBRICATING JELLY, Substantially Equivalent on 1990-10-26. Applicant: Lake Pharmaceutical, Inc.. Device class: 1.

Clearance details

Applicant: Lake Pharmaceutical, Inc.
Product code: Code KMJ
Device class: Class 1
Regulation: 21 CFR 880.6375
Advisory panel: General Hospital
Date received: 1990-08-23
Decision date: 1990-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMJ

K142473 — Lubricating Jelly2015-04-13
K141028 — COLONGLIDE LUBRICANT2014-07-24
K131617 — COLONGLIDE(R) LUBRICANT2013-10-03
K121390 — LUBE JELLY SURINGE2012-08-10
K113689 — DUKAL LUBRICATING JELLY2012-05-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.