meddevicedb.com FDA Device Reference

SWIMEX MULTIDEPTH POOL (MODEL 600T)

K935011 Class I Traditional
Decision Date
1995-01-09
Sponsor / Applicant
Swimex Systems

Technical Specification

510(k) Submission ID K935011
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1995-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SWIMEX MULTIDEPTH POOL (MODEL 600T) received FDA 510(k) clearance under submission number K935011, sponsored by Swimex Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1995-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code BXB and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.