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AUTO ISO-FILTER COLLECTION TUBE CAP

K780303 Class II Traditional
Decision Date
1978-03-30
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K780303
Product Code GJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1978-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTO ISO-FILTER COLLECTION TUBE CAP received FDA 510(k) clearance under submission number K780303, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1978-03-30.

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.