meddevicedb.com FDA Device Reference

ALBUMIN BCP

K844426 Class II Traditional
Decision Date
1985-01-07
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K844426
Product Code CJW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1035
Decision Date 1985-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALBUMIN BCP received FDA 510(k) clearance under submission number K844426, sponsored by Boehringer Mannheim Corp.. 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 1985-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code CJW and 21 CFR 862.1035, within the Clinical Chemistry review panel as a Class II device.