SYNTHALON PI POWDER-FREE SYNTHETIC POLYISOPRENE/POLYCHLOROPRENE EXAMINATION GLOVES MDL 1362-10 TO 1362-44— 510(k) K060733

Substantially Equivalent

Barriermed, Inc.

FDA 510(k) clearance K060733 for SYNTHALON PI POWDER-FREE SYNTHETIC POLYISOPRENE/POLYCHLOROPRENE EXAMINATION GLOVES MDL 1362-10 TO 1362-44, Substantially Equivalent on 2006-04-24. Applicant: Barriermed, Inc..

Clearance details

Applicant: Barriermed, Inc.
Product code: Code LZA
Advisory panel: General Hospital
Date received: 2006-03-20
Decision date: 2006-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Mary, FL, US

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Adverse events under product code LZA

product code LZA

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.