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ACCURUN 140 RUBELLA IGG POSITIVE CONTROL

K972986 Class I Traditional
Decision Date
1997-10-08
Sponsor / Applicant
Boston Biomedica, Inc.

Technical Specification

510(k) Submission ID K972986
Product Code MJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1997-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCURUN 140 RUBELLA IGG POSITIVE CONTROL received FDA 510(k) clearance under submission number K972986, sponsored by Boston Biomedica, 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 1997-10-08.

Classification & Regulation

This clearance is catalogued under FDA product code MJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.