meddevicedb.com FDA Device Reference

GLYCO-SPIN

K792086 Class II Traditional
Decision Date
1979-11-30
Sponsor / Applicant
Applied Clinical Research Laboratories

Technical Specification

510(k) Submission ID K792086
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 1979-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLYCO-SPIN received FDA 510(k) clearance under submission number K792086, sponsored by Applied Clinical Research Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1979-11-30.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.