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GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS

K935070 Class I Traditional
Decision Date
1994-01-25
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K935070
Product Code FCL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1994-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRASPING FORCEPS, BIOPSY FORCEPS, SPOON FORCEPS received FDA 510(k) clearance under submission number K935070, sponsored by KARL STORZ Endoscopy-America, 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 1994-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code FCL and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class I device.