meddevicedb.com FDA Device Reference

NU-BORN BABY BATH KIT

K802366 Traditional
Decision Date
1980-10-10
Sponsor / Applicant
American Hospital Supply Corp.

Technical Specification

510(k) Submission ID K802366
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1980-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NU-BORN BABY BATH KIT received FDA 510(k) clearance under submission number K802366, sponsored by American Hospital Supply Corp.. 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 1980-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.