meddevicedb.com FDA Device Reference

COMPRESSAR DISPOSABLE DISC

K831337 Class II Traditional
Decision Date
1983-07-19
Sponsor / Applicant
Instromedix, Inc.

Technical Specification

510(k) Submission ID K831337
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1983-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPRESSAR DISPOSABLE DISC received FDA 510(k) clearance under submission number K831337, sponsored by Instromedix, 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 1983-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.