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FREEZER TEETHER

K002066 Class II Traditional
Decision Date
2000-09-26
Sponsor / Applicant
Cool Baby, Inc.

Technical Specification

510(k) Submission ID K002066
Product Code KKO
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5550
Decision Date 2000-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FREEZER TEETHER received FDA 510(k) clearance under submission number K002066, sponsored by Cool Baby, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code KKO and 21 CFR 872.5550, within the Dental review panel as a Class II device.