meddevicedb.com FDA Device Reference

MODEL 366-12 ADAPTAID (TM) STEP-DOWN ADAPTER

K871625 Class III Traditional
Decision Date
1987-05-21
Sponsor / Applicant
Intermedics, Inc.

Technical Specification

510(k) Submission ID K871625
Product Code DTB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3680
Decision Date 1987-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 366-12 ADAPTAID (TM) STEP-DOWN ADAPTER received FDA 510(k) clearance under submission number K871625, sponsored by Intermedics, 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 1987-05-21.

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.