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NEONATAL RESTRAINT AND COMFORT SYSTEMS

K943017 Class I Traditional
Decision Date
1995-01-19
Sponsor / Applicant
K.Bowmed, Inc.

Technical Specification

510(k) Submission ID K943017
Product Code FRP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5680
Decision Date 1995-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEONATAL RESTRAINT AND COMFORT SYSTEMS received FDA 510(k) clearance under submission number K943017, sponsored by K.Bowmed, 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 1995-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code FRP and 21 CFR 880.5680, within the General Hospital review panel as a Class I device.