meddevicedb.com FDA Device Reference

VASCULAR GRAFT PROSTH. OF EXP. MICRO.

K801621 Class II Traditional
Decision Date
1980-09-09
Sponsor / Applicant
Impra, Inc.

Technical Specification

510(k) Submission ID K801621
Product Code DSY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3450
Decision Date 1980-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VASCULAR GRAFT PROSTH. OF EXP. MICRO. received FDA 510(k) clearance under submission number K801621, sponsored by Impra, 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 1980-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code DSY and 21 CFR 870.3450, within the Cardiovascular review panel as a Class II device.