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PINTLER PATIENT WARMING SYSTEM

K113705 Class II Traditional
Decision Date
2012-08-31
Sponsor / Applicant
Pintler Medical

Technical Specification

510(k) Submission ID K113705
Product Code DWJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2012-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PINTLER PATIENT WARMING SYSTEM received FDA 510(k) clearance under submission number K113705, sponsored by Pintler Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-08-31.

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.