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CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP

K914015 Class I Traditional
Decision Date
1991-11-21
Sponsor / Applicant
Pilling Co.

Technical Specification

510(k) Submission ID K914015
Product Code GBZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1991-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP received FDA 510(k) clearance under submission number K914015, sponsored by Pilling Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1991-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code GBZ and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.