meddevicedb.com FDA Device Reference

SQUEEZE PLAY

K943730 Class I Traditional
Decision Date
1994-11-28
Sponsor / Applicant
Conair Corp.

Technical Specification

510(k) Submission ID K943730
Product Code IRO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5975
Decision Date 1994-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SQUEEZE PLAY received FDA 510(k) clearance under submission number K943730, sponsored by Conair Corp.. 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 1994-11-28.

Classification & Regulation

This clearance is catalogued under FDA product code IRO and 21 CFR 890.5975, within the Physical Medicine review panel as a Class I device.