meddevicedb.com FDA Device Reference

NOVA AIR FLOATATION SYSTEM

K780502 Class II Traditional
Decision Date
1978-04-10
Sponsor / Applicant
Nova Health Systems, Inc.

Technical Specification

510(k) Submission ID K780502
Product Code FNM
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5550
Decision Date 1978-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVA AIR FLOATATION SYSTEM received FDA 510(k) clearance under submission number K780502, sponsored by Nova Health Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1978-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code FNM and 21 CFR 880.5550, within the General Hospital review panel as a Class II device.