meddevicedb.com FDA Device Reference

SYNCHRON LACTATE REAGENT

K910534 Class I Traditional
Decision Date
1991-04-08
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K910534
Product Code KHP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1450
Decision Date 1991-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON LACTATE REAGENT received FDA 510(k) clearance under submission number K910534, sponsored by Beckman Instruments, 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 1991-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code KHP and 21 CFR 862.1450, within the Clinical Chemistry review panel as a Class I device.