LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS— 510(k) K953813

Name: FDA 510(k) clearance K953813
Creator: U.S. Food and Drug Administration
Published: 1996-07-22

Substantially Equivalent

London International U.S. Holdings, Inc.

FDA 510(k) clearance K953813 for LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS, Substantially Equivalent on 1996-07-22. Applicant: London International U.S. Holdings, Inc.. Device class: 2.

Clearance details

Applicant: London International U.S. Holdings, Inc.
Product code: Code LTZ
Device class: Class 2
Regulation: 21 CFR 884.5310
Advisory panel: Obstetrics/Gynecology
Date received: 1995-08-04
Decision date: 1996-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LTZ

view all

K033163 — CAUTION CONDOMS2004-04-27
K012969 — DOUBLE SPRINGERS NONOXNOL 9 CONDOM2002-06-12
K010178 — SPERMICIDAL LUBRICATED MALE LATEX CONDOM2001-04-27
K003375 — CONTROL MALE CONDOMS OF NATURAL RUBBER LATEX2001-01-28
K001978 — 'ONE TOUCH' LATEX CONDOM WITH NONOXYNOL-92000-08-08

More clearances from London International U.S. Holdings, Inc.

view all

K952415 — DUREX, RAMSES, SHEIK1996-07-15

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