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H-WAVE SPORT

K081998 Class II Traditional
Decision Date
2009-07-09
Sponsor / Applicant
Electronic Waveform Laboratory, Inc.

Technical Specification

510(k) Submission ID K081998
Product Code NGX
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2009-07-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

H-WAVE SPORT received FDA 510(k) clearance under submission number K081998, sponsored by Electronic Waveform Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2009-07-09.

Classification & Regulation

This clearance is catalogued under FDA product code NGX and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.