meddevicedb.com FDA Device Reference

ISCIENCE SURGICAL VISCOINJECTOR

K050716 Class II Traditional
Decision Date
2005-04-21
Sponsor / Applicant
Iscience Surgical Corporation

Technical Specification

510(k) Submission ID K050716
Product Code MRH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2005-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISCIENCE SURGICAL VISCOINJECTOR received FDA 510(k) clearance under submission number K050716, sponsored by Iscience Surgical Corporation. 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 2005-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code MRH and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.