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KARL STORZ TAKE-APART BIOPOLAR FORCEPS

K953809 Class II Traditional
Decision Date
1995-11-06
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K953809
Product Code HET
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1720
Decision Date 1995-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KARL STORZ TAKE-APART BIOPOLAR FORCEPS received FDA 510(k) clearance under submission number K953809, sponsored by KARL STORZ Endoscopy-America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1995-11-06.

Classification & Regulation

This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.