MIGHTY MAN (DYNAMIC LINKERS)— 510(k) K993737

Name: FDA 510(k) clearance K993737
Creator: U.S. Food and Drug Administration
Published: 2000-03-20

Substantially Equivalent

Medtech Products , Ltd.

FDA 510(k) clearance K993737 for MIGHTY MAN (DYNAMIC LINKERS), Substantially Equivalent on 2000-03-20. Applicant: Medtech Products , Ltd.. Device class: 2.

Clearance details

Applicant: Medtech Products , Ltd.
Product code: Code HIS
Device class: Class 2
Regulation: 21 CFR 884.5300
Advisory panel: Obstetrics/Gynecology
Date received: 1999-11-04
Decision date: 2000-03-20
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Chennai, IN

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIS

view all

K252622 — Male Latex Condom HA2026-05-04
K252521 — LifeStyles® HydraFeel Natural Rubber Latex Condom2025-11-18
K250034 — Natural rubber latex male condom2025-07-11
K243421 — Lelo Hex Lubricated Natural Rubber Latex Condom2025-03-07
K243640 — Trojan Ultra Ribbed Ecstasy latex condom with lubricant (Trojan Ultra Ribbed Ecstasy)2025-02-21

More clearances from Medtech Products , Ltd.

view all

K063401 — BANANA RIBBED2007-03-26
K012969 — DOUBLE SPRINGERS NONOXNOL 9 CONDOM2002-06-12
K993733 — LOVE LOCKERS2000-03-20
K993735 — DOUBLE SPRINGERS2000-03-20

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