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LIFE-AIR 1000 HYPOTHERMIC TREATMENT SYSTEM

K914382 Class II Traditional
Decision Date
1992-04-21
Sponsor / Applicant
Progressive Dynamics, Inc.

Technical Specification

510(k) Submission ID K914382
Product Code DWJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 1992-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFE-AIR 1000 HYPOTHERMIC TREATMENT SYSTEM received FDA 510(k) clearance under submission number K914382, sponsored by Progressive Dynamics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1992-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code DWJ and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.