Medical Device Manufacturer · US , Columbia , MD

Surgi-Vision, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1999

Total

Cleared

Denied

Surgi-Vision, Inc. has 9 FDA 510(k) cleared medical devices. Based in Columbia, US.

Historical record: 9 cleared submissions from 1999 to 2011. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Surgi-Vision, Inc.

9 devices

1-9 of 9

Cleared Jun 22, 2011

SURGIVISION INC. CLEARPOINT SYSTEM

K111073 · ORR

Radiology · 65d

Cleared May 21, 2002

INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND...

K020790 · MOS

Radiology · 71d

Cleared Apr 23, 2002

INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL,...

K020495 · MOS

Radiology · 68d

Cleared Aug 31, 2001

INTERCEPT-URETHRAL MICROCOIL

K011781 · MOS

Radiology · 85d

Cleared Feb 02, 2001

SURGI-VISION GUIDEWIRE COIL

K003436 · MOS

Radiology · 88d

Cleared Nov 28, 2000

SURGI-VISION PROSTATE COIL

K002916 · MOS

Radiology · 70d

Cleared Oct 11, 2000

SURGI-VISION URETHRAL COIL

K002345 · MOS

Radiology · 70d

Cleared Mar 14, 2000

SURGI-VISION ESOPHAGEAL STYLET COIL

K994436 · MOS

Radiology · 75d

Cleared Sep 03, 1999

ENDO-ESOPHAGEAL MR COIL

K992193 · MOS

Radiology · 66d

Surgi-Vision, Inc. - FDA 510(k) Cleared Devices

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