meddevicedb.com FDA Device Reference

PROXIMATE LINEAR CUTTER THICK TISSUE INST.

K892927 Class II Traditional
Decision Date
1989-05-26
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K892927
Product Code GAG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 878.4740
Decision Date 1989-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROXIMATE LINEAR CUTTER THICK TISSUE INST. received FDA 510(k) clearance under submission number K892927, sponsored by ETHICON, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1989-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code GAG and 21 CFR 878.4740, within the General Hospital review panel as a Class II device.