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PROCLINIC ONE-STEP DIPSTICK PREGNANCY TEST

K930014 Class II Traditional
Decision Date
1993-03-25
Sponsor / Applicant
Vanguard Biomedical Corp.

Technical Specification

510(k) Submission ID K930014
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1993-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCLINIC ONE-STEP DIPSTICK PREGNANCY TEST received FDA 510(k) clearance under submission number K930014, sponsored by Vanguard Biomedical Corp.. 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 1993-03-25.

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.