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FLO-RESTER DISPOSABLE VESSEL OCCLUDER

K942812 Class II Traditional
Decision Date
1994-08-01
Sponsor / Applicant
Bio-Vascular, Inc.

Technical Specification

510(k) Submission ID K942812
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 1994-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLO-RESTER DISPOSABLE VESSEL OCCLUDER received FDA 510(k) clearance under submission number K942812, sponsored by Bio-Vascular, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1994-08-01.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.