Company · US

Kay Elemetrics Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1999. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
EQL	Laryngostroboscope	2
KLA	Monitor, Esophageal Motility, Anorectal Motility, And Tube	1
KLX	Electroglottograph	1
LLZ	System, Image Processing, Radiological	1

Decided	510(k)	Device and applicant	Code
Aug 13, 1999	K991738	DIGITAL VIDEO RECORDING SYSTEM Kay Elemetrics Corp.	LLZ
Mar 11, 1999	K990240	ELECTROGLOTTOGRAPH Kay Elemetrics Corp.	KLX
Jun 4, 1996	K954798	7100 SWALLOWING WORKSTATION Kay Elemetrics Corp.	KLA
May 28, 1992	K921285	9105 RIGID TELESCOPIC ENDOSCOPE Kay Elemetrics Corp.	EQL
May 28, 1992	K921184	RLS 9100 RHINO-LARYNGEAL STROBOSCOPE Kay Elemetrics Corp.	EQL

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