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MULTI HI-FLO PNEU, WISAP #7080

K011510 Class II Traditional
Decision Date
2002-04-02
Sponsor / Applicant
Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh

Technical Specification

510(k) Submission ID K011510
Product Code HIF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1730
Decision Date 2002-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI HI-FLO PNEU, WISAP #7080 received FDA 510(k) clearance under submission number K011510, sponsored by Wisap Gesellschaft Fur Wissenschaftl. App. Bau Mbh. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2002-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code HIF and 21 CFR 884.1730, within the Obstetrics/Gynecology review panel as a Class II device.