Medical Device Manufacturer · US , Argyle , NY

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

7 submissions · 7 cleared · Since 1988

7

Total

7

Cleared

0

Denied

Mallinckroot, Inc. has 7 FDA 510(k) cleared medical devices. Based in Argyle, US.

Historical record: 7 cleared submissions from 1988 to 1999. Primary specialty: Cardiovascular.

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

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

7 devices

1-7 of 7

Cleared Apr 16, 1999

COPPERHEAD 5 FR. PTA CATHETER, FINCH 4 FR. PTA CATHETER

Cardiovascular · 168d

Cleared Oct 02, 1989

MODIFIED SOFTOUCH INTRODUCER W/HEMO VALVE & SIDE

Cardiovascular · 77d

Cleared May 15, 1989

A-V(TM) SOFTOUCH UHF CARDIAC PIGTAIL

Cardiovascular · 138d

Cleared Mar 14, 1989

ATTACHABLE LANZ (TENTATIVE)

Anesthesiology · 85d

Cleared Feb 22, 1989

SOFTOUCH INTRODUCER W/HEMOSTASIS VALVE & SIDEPORT

Cardiovascular · 141d

Cleared Jan 10, 1989

CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE

Cardiovascular · 80d

Cleared Aug 09, 1988

Gastroenterology & Urology · 81d