meddevicedb.com FDA Device Reference

JOBST EXTREMITY PUMP(R) SYSTEM 7500

K882683 Class II Traditional
Decision Date
1988-09-20
Sponsor / Applicant
Jobst Institute, Inc.

Technical Specification

510(k) Submission ID K882683
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 1988-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JOBST EXTREMITY PUMP(R) SYSTEM 7500 received FDA 510(k) clearance under submission number K882683, sponsored by Jobst Institute, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code JOW and 21 CFR 870.5800, within the Cardiovascular review panel as a Class II device.