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SODIUM CITRATE

K761177 Class II Traditional
Decision Date
1977-01-10
Sponsor / Applicant
Bio/Data Corp.

Technical Specification

510(k) Submission ID K761177
Product Code GJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1977-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SODIUM CITRATE received FDA 510(k) clearance under submission number K761177, sponsored by Bio/Data 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 1977-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code GJE and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.