Company · US

X-Cel X-Ray Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 2000. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (0 in 12 months)

1recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
KPR	System, X-Ray, Stationary	2
IYH	Generator, Dermatological (Grenz Ray), Therapeutic X-Ray	1
IZL	System, X-Ray, Mobile	1
MUH	System, X-Ray, Extraoral Source, Digital	1

Decided	510(k)	Device and applicant	Code
Feb 14, 2000	K993958	IDX-60 INTRAORAL X-RAY X-Cel X-Ray Corp.	MUH
Aug 9, 1993	K930699	M6-M X-Cel X-Ray Corp.	IZL
May 14, 1987	K871116	X-CEL X-RAY MODELS ORT90W, ORT90M AND ORT90R X-Cel X-Ray Corp.	IYH
Jun 23, 1981	K811230	X-CELL X-RAY #'S P-75W/P-75M X-Cel X-Ray Corp.	KPR

Date	Firm and product	Code	Linked 510(k)
Mar 5, 2003	X-Cel X-Ray Corp X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012 Terminated	KPR	None listed