meddevicedb.com FDA Device Reference

RTV SILICONE HAND KNEADABLE PUTTY

K780778 Class II Traditional
Decision Date
1978-05-31
Sponsor / Applicant
Crown Delta Corp.

Technical Specification

510(k) Submission ID K780778
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1978-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RTV SILICONE HAND KNEADABLE PUTTY received FDA 510(k) clearance under submission number K780778, sponsored by Crown Delta 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 1978-05-31.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.