meddevicedb.com FDA Device Reference

SAS HCG-CHECK

K991193 Class II Traditional
Decision Date
1999-05-04
Sponsor / Applicant
Sa Scientific, Inc.

Technical Specification

510(k) Submission ID K991193
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1999-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAS HCG-CHECK received FDA 510(k) clearance under submission number K991193, sponsored by Sa Scientific, Inc.. 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 1999-05-04.

Classification & Regulation

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