3M CARPAL TUNNEL— 510(k) K881703

Substantially Equivalent

3M Company

FDA 510(k) clearance K881703 for 3M CARPAL TUNNEL, Substantially Equivalent on 1988-07-25. Applicant: 3M Company.

Clearance details

Applicant: 3M Company
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 1988-04-19
Decision date: 1988-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cottae Grove, MN, US

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Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.