meddevicedb.com FDA Device Reference

HOMEPUMP NSF

K932740 Class II Traditional
Decision Date
1993-10-06
Sponsor / Applicant
Block Medical, Inc.

Technical Specification

510(k) Submission ID K932740
Product Code MED
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6885
Decision Date 1993-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOMEPUMP NSF received FDA 510(k) clearance under submission number K932740, sponsored by Block Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1993-10-06.

Classification & Regulation

This clearance is catalogued under FDA product code MED and 21 CFR 880.6885, within the General Hospital review panel as a Class II device.