WUNDER TEST— 510(k) K102428

Substantially Equivalent

Hien Helen Nguyen

FDA 510(k) clearance K102428 for WUNDER TEST, Substantially Equivalent on 2012-04-18. Applicant: Hien Helen Nguyen. Device class: 2.

Clearance details

Applicant
Hien Helen Nguyen
Product code
Product code LDJ
Device class
Class 2
Regulation
21 CFR 862.3870
Advisory panel
Clinical Toxicology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Jose, CA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LDJ

view all

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