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VAC-RITE SUNCTION COLLECTION

K811192 Class II Traditional
Decision Date
1981-06-02
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K811192
Product Code KDQ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1981-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VAC-RITE SUNCTION COLLECTION received FDA 510(k) clearance under submission number K811192, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1981-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code KDQ and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.