ClearanceBrief
Company ยท IL

A.Stein - Regulatory Affairs Consulting

FDA 510(k) clearances and medical device recalls filed under this name, 1997 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

CodeDeviceRecords
FWFCamera, Television, Endoscopic, Without Audio1
JOWSleeve, Limb, Compressible1
KLZTube, Shunt, Endolymphatic With Valve1
LKXDevice, Thermal, Hemorrhoids1
LLZSystem, Image Processing, Radiological1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 23, 1999K972383EASY-JET DEVICE
A.Stein - Regulatory Affairs Consulting, IL
KLZ
May 20, 1999K973592WALKCARE P200 SYSTEM
A.Stein - Regulatory Affairs Consulting, IL
JOW
Jan 8, 1999K982754EC-1000-7 DIGITAL ENDOSCOPY VIDEO CAMERA, MODELS EC 1000-7P (PAL) & EC 1000-7N (NTSC)
A.Stein - Regulatory Affairs Consulting, IL
FWF
Feb 5, 1998K973590HEMORRELIEF DEVICE
A.Stein - Regulatory Affairs Consulting, IL
LKX
Nov 20, 1997K973148MACOM
A.Stein - Regulatory Affairs Consulting, IL
LLZ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes