meddevicedb.com FDA Device Reference

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860

K872731 Class III Traditional
Decision Date
1987-09-15
Sponsor / Applicant
Ela Medical, Inc.

Technical Specification

510(k) Submission ID K872731
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1987-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 received FDA 510(k) clearance under submission number K872731, sponsored by Ela Medical, 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 1987-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code DTB and 21 CFR 870.3680, within the Cardiovascular review panel as a Class III device.