meddevicedb.com FDA Device Reference

THROMBOPLATIN-M WITH CALCIUM

K930212 Class II Traditional
Decision Date
1993-05-11
Sponsor / Applicant
Sigma Diagnostics, Inc.

Technical Specification

510(k) Submission ID K930212
Product Code GJS
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7750
Decision Date 1993-05-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THROMBOPLATIN-M WITH CALCIUM received FDA 510(k) clearance under submission number K930212, sponsored by Sigma Diagnostics, 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 1993-05-11.

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.