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APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501

K913098 Class II Traditional
Decision Date
1991-11-05
Sponsor / Applicant
Dlp, Inc.

Technical Specification

510(k) Submission ID K913098
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1991-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501 received FDA 510(k) clearance under submission number K913098, sponsored by Dlp, 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 1991-11-05.

Classification & Regulation

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