MEDTRADE PRODUCTS SILICONE SCAR THERAPY GEL, SPENCO MEDICAL CORP. 2ND SKIN SILICONE SCAR THERAPY GEL, MODEL 09916030.— 510(k) K014036

Name: FDA 510(k) clearance K014036
Creator: U.S. Food and Drug Administration
Published: 2002-02-14

Substantially Equivalent

Medtrade Products , Ltd.

FDA 510(k) clearance K014036 for MEDTRADE PRODUCTS SILICONE SCAR THERAPY GEL, SPENCO MEDICAL CORP. 2ND SKIN SILICONE SCAR THERAPY GEL, MODEL 09916030., Substantially Equivalent on 2002-02-14. Applicant: Medtrade Products , Ltd.. Device class: 1.

Clearance details

Applicant: Medtrade Products , Ltd.
Product code: Code MDA
Device class: Class 1
Regulation: 21 CFR 878.4025
Advisory panel: General, Plastic Surgery
Date received: 2001-12-07
Decision date: 2002-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crewe, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code MDA

view all

K112131 — NEODYNE DRESSING2011-09-29
K111733 — CORELEADER SCAR-DIMMER2011-09-22
K083718 — BEAU RX SCAR CARE GEL2009-01-26
K053481 — KELO-COTE SPRAY2006-04-14
K041704 — NEWGEL AND NEWGEL PLUS E2005-10-17

More clearances from Medtrade Products , Ltd.

view all

K230589 — Celox Rapid X-Ray Gauze2023-11-17
K161274 — Bondiloxs Topical Hemostatic Granules2017-01-18
K132333 — BONDILOXS TOPICAL HEMOSTATIC DRESSING2014-06-25
K120930 — CHG ANTIBACTERIAL FOAM DRESSING, CHG ANTIBACTERIAL PATCH, CHG ANTIBACTERIAL FOAM PATCH, CHG PATCH, CHG DRESSING2012-10-26
K113560 — CELOX GAUZE PRO2012-08-01

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