LEEDAR (PATIENT EXAMINATION GLOVES - LATEX)— 510(k) K891663

Substantially Equivalent

Darchet (Usa), Inc.

FDA 510(k) clearance K891663 for LEEDAR (PATIENT EXAMINATION GLOVES - LATEX), Substantially Equivalent on 1990-02-13. Applicant: Darchet (Usa), Inc..

Clearance details

Applicant: Darchet (Usa), Inc.
Product code: Code LYY
Advisory panel: General Hospital
Date received: 1989-03-20
Decision date: 1990-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monterey Park, CA, US

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