REGENECARE WOUND GEL— 510(k) K020540

Name: FDA 510(k) clearance K020540
Creator: U.S. Food and Drug Administration
Published: 2002-11-01

Substantially Equivalent

Mpm Medical., Inc.

FDA 510(k) clearance K020540 for REGENECARE WOUND GEL, Substantially Equivalent on 2002-11-01. Applicant: Mpm Medical., Inc.. Device class: Unclassified.

Clearance details

Applicant: Mpm Medical., Inc.
Product code: Code SEJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-02-19
Decision date: 2002-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irving, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code SEJ

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K092086 — AMERIGEL WOUND DRESSING PLUS 1/2 OZ. (15G TUBE), MODEL A2025; 1 OZ. (30G TUBE), MODEL A2026; 3 OZ (90G TUBE),MODEL A20272009-07-30
K053476 — ALLWOUND2006-06-26
K001023 — FREEDOM, MODEL 46602000-09-22
K922636 — HEMO-STAT1992-11-09
K912565 — MICRO-COLL COLLAGEN WOUND SPRAY1992-06-11

More clearances from Mpm Medical., Inc.

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K060340 — ORAMAGIC PLUS ORAL WOUND RINSE2006-05-10
K024180 — ORAMAGICRX ORAL WOUND RINSE2003-03-14
K992074 — MPM REGENECARE WOUND GEL1999-12-23
K962160 — MPM HYDROGEL DRESSING (NON-STERILE)1996-06-26
K952276 — MPM HYDROGEL DRESSING1995-06-30

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