meddevicedb.com FDA Device Reference

GELMAN LIPOPROTEIN FRS SET. P/N 51213

K791606 Class I Traditional
Decision Date
1979-09-17
Sponsor / Applicant
Gelman Sciences, Inc.

Technical Specification

510(k) Submission ID K791606
Product Code JHO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1475
Decision Date 1979-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GELMAN LIPOPROTEIN FRS SET. P/N 51213 received FDA 510(k) clearance under submission number K791606, sponsored by Gelman Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1979-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code JHO and 21 CFR 862.1475, within the Clinical Chemistry review panel as a Class I device.