meddevicedb.com FDA Device Reference

MC INFANT CARE UNIE #PP30

K950059 Class II Traditional
Decision Date
1995-02-10
Sponsor / Applicant
Janco Consulting Services

Technical Specification

510(k) Submission ID K950059
Product Code FMS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5140
Decision Date 1995-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MC INFANT CARE UNIE #PP30 received FDA 510(k) clearance under submission number K950059, sponsored by Janco Consulting Services. 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 1995-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code FMS and 21 CFR 880.5140, within the General Hospital review panel as a Class II device.