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SILICONE ELASTOMER KIT

K810869 Class II Traditional
Decision Date
1981-04-29
Sponsor / Applicant
Rapid Injection Systems Corp.

Technical Specification

510(k) Submission ID K810869
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 1981-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILICONE ELASTOMER KIT received FDA 510(k) clearance under submission number K810869, sponsored by Rapid Injection Systems 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 1981-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.