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EMATOLOGY DILUENT RESERVOIR CLOSURE

K770980 Class I Traditional
Decision Date
1977-07-11
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K770980
Product Code GHO
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6160
Decision Date 1977-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMATOLOGY DILUENT RESERVOIR CLOSURE received FDA 510(k) clearance under submission number K770980, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1977-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code GHO and 21 CFR 864.6160, within the Hematology review panel as a Class I device.