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HOBBS MEDICAL/JAYCO ASPIRATION CATHETER

K844550 Class II Traditional
Decision Date
1985-01-03
Sponsor / Applicant
Hobbs Medical, Inc.

Technical Specification

510(k) Submission ID K844550
Product Code OCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1985-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOBBS MEDICAL/JAYCO ASPIRATION CATHETER received FDA 510(k) clearance under submission number K844550, sponsored by Hobbs 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 1985-01-03.

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.