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J-VAC SUCTION RESERVOIRS & J-VAC BLAKE SILICONE DRAINS

K953655 Class II Traditional
Decision Date
1995-10-13
Sponsor / Applicant
Johnson & Johnson Medical, Inc.

Technical Specification

510(k) Submission ID K953655
Product Code OCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1995-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

J-VAC SUCTION RESERVOIRS & J-VAC BLAKE SILICONE DRAINS received FDA 510(k) clearance under submission number K953655, sponsored by Johnson & Johnson Medical, 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 1995-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code OCX and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.