DeviceClearance

PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K892107

Substantially Equivalent

Success Development (Usa) Co., Inc.

FDA 510(k) clearance K892107 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1989-09-13. Applicant: Success Development (Usa) Co., Inc..

Clearance details

Applicant
Success Development (Usa) Co., Inc.
Product code
Code LYY
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Los Angeles, CA, US
Download summary PDFView on FDA.gov ↗

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