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RITTER MODEL H COMPANION STOOL

K800276 Class I Traditional
Decision Date
1980-03-17
Sponsor / Applicant
Sybron Corp.

Technical Specification

510(k) Submission ID K800276
Product Code KLC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6250
Decision Date 1980-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RITTER MODEL H COMPANION STOOL received FDA 510(k) clearance under submission number K800276, sponsored by Sybron 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 1980-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code KLC and 21 CFR 872.6250, within the Dental review panel as a Class I device.