MULTIDEX HYDROPHILIC WOUND DRESSING GEL— 510(k) K962917

Name: FDA 510(k) clearance K962917
Creator: U.S. Food and Drug Administration
Published: 1996-12-16

Substantially Equivalent for Some Indications

Lange Medical Products, Inc.

FDA 510(k) clearance K962917 for MULTIDEX HYDROPHILIC WOUND DRESSING GEL, Substantially Equivalent for Some Indications on 1996-12-16. Applicant: Lange Medical Products, Inc.. Device class: Unclassified.

Clearance details

Applicant: Lange Medical Products, Inc.
Product code: Code MGQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1996-07-26
Decision date: 1996-12-16
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Wheeling, IL, US

Download summary PDF View on FDA.gov ↗

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K955399 — MULTIDEX PLUS HYDROPHILIC WOUND DRESSING1996-02-07
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Adverse events under product code MGQ

product code MGQ

Death: 16
Total: 16

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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