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VARELISA RECOMBI ANA PROFILE

K993109 Class II Traditional
Decision Date
1999-11-12
Sponsor / Applicant
Pharmacia & Upjohn Co.

Technical Specification

510(k) Submission ID K993109
Product Code LJM
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 1999-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VARELISA RECOMBI ANA PROFILE received FDA 510(k) clearance under submission number K993109, 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 1999-11-12.

Classification & Regulation

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