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SIMPLEX AIRBRATOR (SAB-7)

K980672 Class II Traditional
Decision Date
2000-05-04
Sponsor / Applicant
Irt Management Corp.

Technical Specification

510(k) Submission ID K980672
Product Code KOJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6080
Decision Date 2000-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIMPLEX AIRBRATOR (SAB-7) received FDA 510(k) clearance under submission number K980672, sponsored by Irt Management Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code KOJ and 21 CFR 872.6080, within the Dental review panel as a Class II device.