meddevicedb.com FDA Device Reference

BOEHRINGER MANNHEIM BICARBONATE ASSAY

K933461 Class II Traditional
Decision Date
1994-12-05
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K933461
Product Code KHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 1994-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOEHRINGER MANNHEIM BICARBONATE ASSAY received FDA 510(k) clearance under submission number K933461, 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 1994-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code KHS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.