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ENZYMATIC BUN (RATE) REAGENT KIT

K761261 Class II Traditional
Decision Date
1976-12-29
Sponsor / Applicant
Beckman Instruments, Inc.

Technical Specification

510(k) Submission ID K761261
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1976-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZYMATIC BUN (RATE) REAGENT KIT received FDA 510(k) clearance under submission number K761261, 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 1976-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code CDQ and 21 CFR 862.1770, within the Clinical Chemistry review panel as a Class II device.