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THERMOSUIT SYSTEM

K061023 Class II Traditional
Decision Date
2006-09-20
Sponsor / Applicant
Life Recovery Systems Hd, LLC

Technical Specification

510(k) Submission ID K061023
Product Code NZE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2006-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERMOSUIT SYSTEM received FDA 510(k) clearance under submission number K061023, sponsored by Life Recovery Systems Hd, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-09-20.

Classification & Regulation

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