Company · US

Bay X-Ray, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1988. 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
IXR	Table, Radiographic, Tilting	2
IZO	Generator, High-Voltage, X-Ray, Diagnostic	1
JAA	System, X-Ray, Fluoroscopic, Image-Intensified	1
KPR	System, X-Ray, Stationary	1
KXJ	Table, Radiologic	1

Decided	510(k)	Device and applicant	Code
Oct 21, 1988	K883161	HIMOBILIX 2N Bay X-Ray, Inc.	JAA
Sep 8, 1988	K883160	CATAPULT BUCKY (KATAPULT BLENDA) Bay X-Ray, Inc.	KPR
Sep 6, 1988	K883162	TELESTATIX X-RAY TABLE Bay X-Ray, Inc.	IXR
Sep 6, 1988	K883155	RASTIX X-RAY TABLE Bay X-Ray, Inc.	KXJ
Sep 6, 1988	K883154	SELDIX 325 TWO PULSE GENERATOR/CONTROL Bay X-Ray, Inc.	IZO
Sep 6, 1988	K883153	UNDISTAT WITH EXPLORATOR 35 (UCS 35E) Bay X-Ray, Inc.	IXR

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