meddevicedb.com FDA Device Reference

MODEL WC-115 MOBILE BASSINET

K884285 Class II Traditional
Decision Date
1988-12-22
Sponsor / Applicant
Gempco, Inc.

Technical Specification

510(k) Submission ID K884285
Product Code FMT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5130
Decision Date 1988-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL WC-115 MOBILE BASSINET received FDA 510(k) clearance under submission number K884285, sponsored by Gempco, Inc.. 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 1988-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code FMT and 21 CFR 880.5130, within the General Hospital review panel as a Class II device.