PATIENT EXAMINATION GLOVES (LATEX)— 510(k) K891662

Substantially Equivalent

Darchet (Usa), Inc.

FDA 510(k) clearance K891662 for PATIENT EXAMINATION GLOVES (LATEX), Substantially Equivalent on 1990-01-26. Applicant: Darchet (Usa), Inc.. Device class: 1.

Clearance details

Applicant
Darchet (Usa), Inc.
Product code
Code LYY
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Monterey Park, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LYY

view all

More clearances from Darchet (Usa), Inc.

view all

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