meddevicedb.com FDA Device Reference

SYRIGENE ACETIC ACID PRE-FILLEDSYRINGE

K935643 Class II Traditional
Decision Date
1994-06-10
Sponsor / Applicant
Regulatory & Marketing Services, Inc.

Technical Specification

510(k) Submission ID K935643
Product Code KNY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1994-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYRIGENE ACETIC ACID PRE-FILLEDSYRINGE received FDA 510(k) clearance under submission number K935643, sponsored by Regulatory & Marketing Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1994-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code KNY and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.