MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES— 510(k) K013604

Substantially Equivalent

Ansell Healthcare Products, Inc.

FDA 510(k) clearance K013604 for MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES, Substantially Equivalent on 2001-11-13. Applicant: Ansell Healthcare Products, Inc..

Clearance details

Applicant: Ansell Healthcare Products, Inc.
Product code: Code KGO
Advisory panel: General, Plastic Surgery
Date received: 2001-10-31
Decision date: 2001-11-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Massillon, OH, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.