meddevicedb.com FDA Device Reference

HEMAWIPE SYSTEM, THE CIVILIZED TEST

K884206 Class II Traditional
Decision Date
1989-04-18
Sponsor / Applicant
Labeltape Meditect, Inc.

Technical Specification

510(k) Submission ID K884206
Product Code KHE
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6550
Decision Date 1989-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMAWIPE SYSTEM, THE CIVILIZED TEST received FDA 510(k) clearance under submission number K884206, sponsored by Labeltape Meditect, 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 1989-04-18.

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.