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RANGE OF CROCODILE ACTION INSTRUMENTS

K873934 Class I Traditional
Decision Date
1987-12-17
Sponsor / Applicant
Downs Surgical , Ltd.

Technical Specification

510(k) Submission ID K873934
Product Code GZX
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4525
Decision Date 1987-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RANGE OF CROCODILE ACTION INSTRUMENTS received FDA 510(k) clearance under submission number K873934, sponsored by Downs Surgical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1987-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code GZX and 21 CFR 882.4525, within the Neurology review panel as a Class I device.