ARJOWRAP 47/100 AND 47/88— 510(k) K062100

Substantially Equivalent

Arjo Wiggins Medical, Inc.

FDA 510(k) clearance K062100 for ARJOWRAP 47/100 AND 47/88, Substantially Equivalent on 2006-12-05. Applicant: Arjo Wiggins Medical, Inc..

Clearance details

Applicant: Arjo Wiggins Medical, Inc.
Product code: Code FRG
Advisory panel: General Hospital
Date received: 2006-07-24
Decision date: 2006-12-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Appollo Beach, FL, US

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Adverse events under product code FRG

product code FRG

Other: 3
Total: 3

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.