ORIENT, LATEX SURGICAL GLOVES, STERILE— 510(k) K884882

Name: FDA 510(k) clearance K884882
Creator: U.S. Food and Drug Administration
Published: 1989-05-24

Substantially Equivalent

Rosa Intl.

FDA 510(k) clearance K884882 for ORIENT, LATEX SURGICAL GLOVES, STERILE, Substantially Equivalent on 1989-05-24. Applicant: Rosa Intl.. Device class: 1.

Clearance details

Applicant: Rosa Intl.
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1988-11-22
Decision date: 1989-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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