MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045— 510(k) K002599

Substantially Equivalent

Acrymed, Inc.

FDA 510(k) clearance K002599 for MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045, Substantially Equivalent on 2000-09-21. Applicant: Acrymed, Inc..

Clearance details

Applicant: Acrymed, Inc.
Product code: Code FRO
Advisory panel: Unknown
Date received: 2000-08-21
Decision date: 2000-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

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Adverse events under product code FRO

product code FRO

Death: 30
Injury: 653
Malfunction: 479
Other: 11
Total: 1,173

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.