KTI TRANSPARENT WOUND DRESSING— 510(k) K925660

Substantially Equivalent

Kingston Technologies, Inc.

FDA 510(k) clearance K925660 for KTI TRANSPARENT WOUND DRESSING, Substantially Equivalent on 1993-04-20. Applicant: Kingston Technologies, Inc..

Clearance details

Applicant: Kingston Technologies, Inc.
Product code: Code MGP
Advisory panel: Unknown
Date received: 1992-11-10
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dayton, NJ, US

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Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

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.