PATIENT EXAMINATION GLOVES— 510(k) K895617

Substantially Equivalent

Lit Seng Development Sdn. Bhd.

FDA 510(k) clearance K895617 for PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1990-01-22. Applicant: Lit Seng Development Sdn. Bhd.. Device class: 1.

Clearance details

Applicant
Lit Seng Development Sdn. Bhd.
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
S.D.E., West Malaysia, MY
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.