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BORNING NEONATAL RESUSCITATOIN CENTER

K850069 Class II Traditional
Decision Date
1985-05-30
Sponsor / Applicant
Borning Corp.

Technical Specification

510(k) Submission ID K850069
Product Code FMT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5130
Decision Date 1985-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BORNING NEONATAL RESUSCITATOIN CENTER received FDA 510(k) clearance under submission number K850069, sponsored by Borning 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 1985-05-30.

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.