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OVUSIGN LH/CONCEPTION PLUS/OVUDATE LH ONE-STEP

K930185 Class I Traditional
Decision Date
1993-03-04
Sponsor / Applicant
Princeton Biomedix

Technical Specification

510(k) Submission ID K930185
Product Code CEP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1485
Decision Date 1993-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OVUSIGN LH/CONCEPTION PLUS/OVUDATE LH ONE-STEP received FDA 510(k) clearance under submission number K930185, sponsored by Princeton Biomedix. 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 1993-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code CEP and 21 CFR 862.1485, within the Clinical Chemistry review panel as a Class I device.