meddevicedb.com FDA Device Reference

VARELISA SM ANTIBODIES

K000312 Class II Traditional
Decision Date
2000-03-17
Sponsor / Applicant
Pharmacia & Upjohn Co.

Technical Specification

510(k) Submission ID K000312
Product Code LKP
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 2000-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VARELISA SM ANTIBODIES received FDA 510(k) clearance under submission number K000312, sponsored by Pharmacia & Upjohn Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code LKP and 21 CFR 866.5100, within the Immunology review panel as a Class II device.