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LITTLE ANGELS SWADDLING BLANKET

K123411 Class II Traditional
Decision Date
2013-03-07
Sponsor / Applicant
Bionix Development Corp.

Technical Specification

510(k) Submission ID K123411
Product Code PDH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 2013-03-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LITTLE ANGELS SWADDLING BLANKET received FDA 510(k) clearance under submission number K123411, sponsored by Bionix Development 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 2013-03-07.

Classification & Regulation

This clearance is catalogued under FDA product code PDH and 21 CFR 880.5700, within the General Hospital review panel as a Class II device.