TROJAN POLYURETHANE CONDOM (MODIFICATION)— 510(k) K955672

Name: FDA 510(k) clearance K955672
Creator: U.S. Food and Drug Administration
Published: 1996-08-29

Substantially Equivalent

Carter Products

FDA 510(k) clearance K955672 for TROJAN POLYURETHANE CONDOM (MODIFICATION), Substantially Equivalent on 1996-08-29. Applicant: Carter Products. Device class: 2.

Clearance details

Applicant: Carter Products
Product code: Code MOL
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1995-11-01
Decision date: 1996-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cranbury, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MOL

view all

K252158 — Sagami Original 002 Polyurethane Male Condom2026-03-30
K243967 — ONE Nitrile Condom2025-04-08
K241617 — Durex Polyisoprene Condom2025-02-28
K240379 — TROJAN SIS Synthetic Latex Condom with Silicone Lubricant2024-10-08
K240896 — ONE Nitrile Condom2024-08-23

More clearances from Carter Products

view all

K942697 — TROJAN POLYURETHANE CONDOM1995-06-22
K912901 — TROJAN (TM-TBD) CONDOM1992-02-03
K904782 — ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST1990-12-06
K904273 — MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.1990-10-31
K901202 — TROJAN NATURALAMB LUBRICATED NATURAL MODIFIED1990-06-19

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