ClearanceBrief
Company ยท US

Angiolaz, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2000. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FWFCamera, Television, Endoscopic, Without Audio3
LYKAngioscope2
FCWLight Source, Fiberoptic, Routine1
FETEndoscopic Video Imaging System/Component, Gastroenterology-Urology1
FSRLight, Headband, Surgical1
FSSLight, Surgical, Floor Standing1
GCTLight Source, Endoscope, Xenon Arc1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 11, 2000K994362HEADLAMP HL2000.
Angiolaz, Inc.
FSR
Oct 20, 1999K99244750 W METAL HALIDE ILLUMINATOR, VES 0501.
Angiolaz, Inc.
FCW
Sep 10, 1998K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM
Angiolaz, Inc.
FWF
Aug 21, 1998K982409VES 1501-M
Angiolaz, Inc.
FWF
Aug 4, 1998K981819ANGIOLAZ VES-1CAM
Angiolaz, Inc.
FWF
Jul 29, 1998K981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR
Angiolaz, Inc.
FSS
Jul 28, 1998K981827VES 0281-M COMPLETE VIDEO ENDOSCOPIC VIDEO SYSTEM
Angiolaz, Inc.
FET
Nov 10, 1993K933868ANGIOLAZ VIDEO ENDOSCOPIC SYSTEM MODEL CAMLUM1 AND ACCESSORIES
Angiolaz, Inc.
GCT
Dec 27, 1991K913129ANGIOLAZ ANGIOSCOPE CATHETER
Angiolaz, Inc.
LYK
Aug 22, 1990K902329ULTRA-VU ANGIOSCOPE
Angiolaz, Inc.
LYK

Latest recalls

DateFirm and productCodeLinked 510(k)
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