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CIT BIOPSY PUNCHES

K944444 Class I Traditional
Decision Date
1995-09-29
Sponsor / Applicant
Chirurgische Instrumente

Technical Specification

510(k) Submission ID K944444
Product Code HFB
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4530
Decision Date 1995-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIT BIOPSY PUNCHES received FDA 510(k) clearance under submission number K944444, sponsored by Chirurgische Instrumente. 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 1995-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code HFB and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class I device.