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PARAPODIUM

K791565 Class I Traditional
Decision Date
1979-08-28
Sponsor / Applicant
Physico-Medical Systems Corp.

Technical Specification

510(k) Submission ID K791565
Product Code IQI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1979-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARAPODIUM received FDA 510(k) clearance under submission number K791565, sponsored by Physico-Medical Systems 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 1979-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code IQI and 21 CFR 890.3475, within the Physical Medicine review panel as a Class I device.