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Company · US

Electronic Waveform Laboratory, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 2011. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
IPF	Stimulator, Muscle, Powered	2
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	1
KZM	Device, Muscle Monitoring	1
LWM	Device, Electrical Dental Anesthesia	1
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jun 1, 2011	K103738	H-WAVE Electronic Waveform Laboratory, Inc.	IPF
Jul 9, 2009	K081998	H-WAVE SPORT Electronic Waveform Laboratory, Inc.	NGX
May 8, 1992	K915230	H WAVE MUSCLE STIMULATOR Electronic Waveform Laboratory, Inc.	IPF
Apr 12, 1988	K873604	E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY Electronic Waveform Laboratory, Inc.	LWM
Jun 17, 1987	K862121	E.W.L. P-TENS/H-WAVE Electronic Waveform Laboratory, Inc.	KZM
Mar 19, 1982	K813601	E.W.L. P-TENS MODEL(TENS Electronic Waveform Laboratory, Inc.	GZJ

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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