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ARTERIAL BLOOD FILTER AF-1025-AF-1025BL

K830131 Class II Traditional
Decision Date
1983-01-28
Sponsor / Applicant
American Bentley

Technical Specification

510(k) Submission ID K830131
Product Code DTM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4260
Decision Date 1983-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARTERIAL BLOOD FILTER AF-1025-AF-1025BL received FDA 510(k) clearance under submission number K830131, sponsored by American Bentley. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1983-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code DTM and 21 CFR 870.4260, within the Cardiovascular review panel as a Class II device.