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1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE

K851748 Class I Traditional
Decision Date
1985-06-13
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851748
Product Code GWZ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1700
Decision Date 1985-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE received FDA 510(k) clearance under submission number K851748, sponsored by Artiberia. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1985-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code GWZ and 21 CFR 882.1700, within the Neurology review panel as a Class I device.