meddevicedb.com FDA Device Reference

TISSUE FORCEPS, VARIOUS TYPES

K891896 Class I Traditional
Decision Date
1989-04-12
Sponsor / Applicant
Zinnanti Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K891896
Product Code GEN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1989-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE FORCEPS, VARIOUS TYPES received FDA 510(k) clearance under submission number K891896, sponsored by Zinnanti Surgical Instruments, 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 1989-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code GEN and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.