Medical Device Manufacturer · US , Rockingham , VT

Angiolaz, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1990

Total

Cleared

Denied

Angiolaz, Inc. has 10 FDA 510(k) cleared medical devices. Based in Rockingham, US.

Historical record: 10 cleared submissions from 1990 to 2000. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Angiolaz, Inc. Filter by specialty or product code using the sidebar.

Angiolaz, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Angiolaz, Inc.

10 devices

1-10 of 10

50 W METAL HALIDE ILLUMINATOR, VES 0501.

K992447 · FCW

Gastroenterology & Urology · 90d

Cleared Sep 10, 1998

VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM

K982397 · FWF

General & Plastic Surgery · 63d

Cleared Aug 21, 1998

VES 1501-M

K982409 · FWF

General & Plastic Surgery · 42d

Cleared Aug 04, 1998

ANGIOLAZ VES-1CAM

K981819 · FWF

General & Plastic Surgery · 74d

Cleared Jul 29, 1998

VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR

K981821 · FSS

General & Plastic Surgery · 68d

Cleared Jul 28, 1998

VES 0281-M COMPLETE VIDEO ENDOSCOPIC VIDEO SYSTEM

K981827 · FET

Gastroenterology & Urology · 67d

Cleared Nov 10, 1993

ANGIOLAZ VIDEO ENDOSCOPIC SYSTEM MODEL CAMLUM1 AND ACCESSORIES

K933868 · GCT

Gastroenterology & Urology · 96d

Cleared Dec 27, 1991

ANGIOLAZ ANGIOSCOPE CATHETER

K913129 · LYK

Cardiovascular · 164d

Angiolaz, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Angiolaz, Inc.

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