PROTEX LATEX EXAMINATION GLOVE— 510(k) K900790

Substantially Equivalent

Seyen Intl., Inc.

FDA 510(k) clearance K900790 for PROTEX LATEX EXAMINATION GLOVE, Substantially Equivalent on 1990-04-05. Applicant: Seyen Intl., Inc..

Clearance details

Applicant: Seyen Intl., Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1990-02-20
Decision date: 1990-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monterey Park, CA, US

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