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NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM

K010031 Class II Special
Decision Date
2001-03-20
Sponsor / Applicant
Wescor, Inc.

Technical Specification

510(k) Submission ID K010031
Product Code KTB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5525
Decision Date 2001-03-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K010031, sponsored by Wescor, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2001-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code KTB and 21 CFR 890.5525, within the Physical Medicine review panel as a Class II device.