meddevicedb.com FDA Device Reference

SURGICAL RULER AND PEN

K790084 Class I Traditional
Decision Date
1979-02-26
Sponsor / Applicant
Devon Industries, Inc.

Technical Specification

510(k) Submission ID K790084
Product Code FZZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4660
Decision Date 1979-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL RULER AND PEN received FDA 510(k) clearance under submission number K790084, sponsored by Devon Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1979-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code FZZ and 21 CFR 878.4660, within the General, Plastic Surgery review panel as a Class I device.