meddevicedb.com FDA Device Reference

MICRO21 WITH CEREBROSPINAL FLUID

K971470 Class II Traditional
Decision Date
1997-09-16
Sponsor / Applicant
Triangle Biomedical Sciences, Inc.

Technical Specification

510(k) Submission ID K971470
Product Code JOY
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5260
Decision Date 1997-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO21 WITH CEREBROSPINAL FLUID received FDA 510(k) clearance under submission number K971470, sponsored by Triangle Biomedical Sciences, 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 1997-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code JOY and 21 CFR 864.5260, within the Hematology review panel as a Class II device.