POWDERED LATEX PATIENT EXAMINATION GLOVES— 510(k) K051913

Substantially Equivalent

Shinemound Enterprise, Inc.

FDA 510(k) clearance K051913 for POWDERED LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 2005-09-30. Applicant: Shinemound Enterprise, Inc..

Clearance details

Applicant: Shinemound Enterprise, Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 2005-07-15
Decision date: 2005-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Billerica, MA, US

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