meddevicedb.com FDA Device Reference

SUPPORT

K810479 Class II Traditional
Decision Date
1981-03-17
Sponsor / Applicant
Sci-Pharm, Inc.

Technical Specification

510(k) Submission ID K810479
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 1981-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPPORT received FDA 510(k) clearance under submission number K810479, sponsored by Sci-Pharm, 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 1981-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.