meddevicedb.com FDA Device Reference

SARNS DELPHIN BASE ADAPTER WITH MINI-BATTERY

K900601 Class II Traditional
Decision Date
1990-03-28
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K900601
Product Code KFM
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4360
Decision Date 1990-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SARNS DELPHIN BASE ADAPTER WITH MINI-BATTERY received FDA 510(k) clearance under submission number K900601, sponsored by 3M Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1990-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code KFM and 21 CFR 870.4360, within the Cardiovascular review panel as a Class II device.