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POLY-LEC SYSTEM

K792582 Class II Traditional
Decision Date
1980-01-16
Sponsor / Applicant
Gamma Biologicals, Inc.

Technical Specification

510(k) Submission ID K792582
Product Code KSI
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.9550
Decision Date 1980-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POLY-LEC SYSTEM received FDA 510(k) clearance under submission number K792582, sponsored by Gamma Biologicals, 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 1980-01-16.

Classification & Regulation

This clearance is catalogued under FDA product code KSI and 21 CFR 864.9550, within the Hematology review panel as a Class II device.