meddevicedb.com FDA Device Reference

HEMOSURE ONE-STEP FECAL OCCULT BLOOD TEST

K041202 Class II Traditional
Decision Date
2004-08-12
Sponsor / Applicant
W.H.P.M., Inc.

Technical Specification

510(k) Submission ID K041202
Product Code KHE
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6550
Decision Date 2004-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOSURE ONE-STEP FECAL OCCULT BLOOD TEST received FDA 510(k) clearance under submission number K041202, sponsored by W.H.P.M., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2004-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code KHE and 21 CFR 864.6550, within the Hematology review panel as a Class II device.