meddevicedb.com FDA Device Reference

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2

K861890 Class I Traditional
Decision Date
1986-06-03
Sponsor / Applicant
Richard-Allan Medical Ind., Inc.

Technical Specification

510(k) Submission ID K861890
Product Code PPM
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 864.4010
Decision Date 1986-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

100%, 95%, 80% & 70% DEHYDRANT CUSTOM BLEND NO. 2 received FDA 510(k) clearance under submission number K861890, sponsored by Richard-Allan Medical Ind., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1986-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code PPM and 21 CFR 864.4010, within the Pathology review panel as a Class I device.