meddevicedb.com FDA Device Reference

BMT ANSCORE HEALTH MANAGEMENT SYSTEM

K993875 Class II Traditional
Decision Date
2000-08-11
Sponsor / Applicant
Boston Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K993875
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 2000-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BMT ANSCORE HEALTH MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K993875, sponsored by Boston Medical Technologies, 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 2000-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.