meddevicedb.com FDA Device Reference

NICE PACK

K832193 Class I Traditional
Decision Date
1983-08-31
Sponsor / Applicant
Universal Medical Instrument Corp.

Technical Specification

510(k) Submission ID K832193
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1983-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NICE PACK received FDA 510(k) clearance under submission number K832193, sponsored by Universal Medical Instrument 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 1983-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code IME and 21 CFR 890.5700, within the Physical Medicine review panel as a Class I device.