meddevicedb.com FDA Device Reference

BLACHLY BITE BLOK & CHEEK FILLER

K770090 Class II Traditional
Decision Date
1977-01-31
Sponsor / Applicant
P.H. Blachly, M.D.

Technical Specification

510(k) Submission ID K770090
Product Code JXL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5070
Decision Date 1977-01-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLACHLY BITE BLOK & CHEEK FILLER received FDA 510(k) clearance under submission number K770090, sponsored by P.H. Blachly, M.D.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1977-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code JXL and 21 CFR 882.5070, within the Neurology review panel as a Class II device.