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SYMBIOSIS BIPOLAR SCISSORS

K950286 Class II Traditional
Decision Date
1995-02-03
Sponsor / Applicant
Symbiosis Corp.

Technical Specification

510(k) Submission ID K950286
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1995-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYMBIOSIS BIPOLAR SCISSORS received FDA 510(k) clearance under submission number K950286, sponsored by Symbiosis Corp.. 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 1995-02-03.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.