DIGIFLEX, LATEX PATIENT EXAMINATION GLOVES— 510(k) K910542

Substantially Equivalent

21st Century Group

FDA 510(k) clearance K910542 for DIGIFLEX, LATEX PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1991-02-19. Applicant: 21st Century Group. Device class: 1.

Clearance details

Applicant
21st Century Group
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
Boston, MA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LYY

view all

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