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WUNDER PREGNANCY TEST

K130456 Class II Traditional
Decision Date
2014-04-08
Sponsor / Applicant
James Nguyen

Technical Specification

510(k) Submission ID K130456
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2014-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WUNDER PREGNANCY TEST received FDA 510(k) clearance under submission number K130456, sponsored by James Nguyen. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2014-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.