meddevicedb.com FDA Device Reference

ACS ULTRA-1 THROMBOPLASTIN

K913249 Class II Traditional
Decision Date
1991-12-04
Sponsor / Applicant
Analytical Control Systems, Inc.

Technical Specification

510(k) Submission ID K913249
Product Code GJS
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7750
Decision Date 1991-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACS ULTRA-1 THROMBOPLASTIN received FDA 510(k) clearance under submission number K913249, sponsored by Analytical Control Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1991-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code GJS and 21 CFR 864.7750, within the Hematology review panel as a Class II device.