meddevicedb.com FDA Device Reference

SHAVE PREP KITS

K842989 Class I Traditional
Decision Date
1984-12-04
Sponsor / Applicant
Biological & Environmental Control Laboratories

Technical Specification

510(k) Submission ID K842989
Product Code KME
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6060
Decision Date 1984-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHAVE PREP KITS received FDA 510(k) clearance under submission number K842989, sponsored by Biological & Environmental Control Laboratories. 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 1984-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code KME and 21 CFR 880.6060, within the General Hospital review panel as a Class I device.