Medical Device Manufacturer · US , Mchenry , IL

Medi-Plast Intl., Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1981

Total

Cleared

Denied

Medi-Plast Intl., Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1981 to 1996. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Medi-Plast Intl., Inc.

12 devices

1-12 of 12

Cleared Feb 12, 1996

MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)

K954284 · DTL

Cardiovascular · 166d

Cleared Oct 23, 1987

10CC CONTROL SYRINGE

K873588 · FMF

General Hospital · 49d

Cleared Oct 22, 1986

MEDI-PLAST DISPOSABLE MANIFOLD

ARTERIAL-VENOUS COMPRESSION DRESSING

K851489

General & Plastic Surgery · 57d

Cleared Jul 06, 1984

STERILE PAN SET

K842136 · FRG

General Hospital · 37d

Cleared Mar 15, 1984

OPERATING ROOM TRAY SET

K840021 · FSM

General & Plastic Surgery · 70d

Cleared Feb 04, 1984

HEART CATHETERIZATION TRAY SET

General Hospital · 45d

Cleared Jun 18, 1981

BOTTLE-TO-BOTTLE

K811268 · KPE

General Hospital · 44d

Cleared Jun 17, 1981

I.V. PLASTIC BAG

K811233 · KPE

General Hospital · 44d

Cleared Jun 16, 1981

GLASS VIALS

K811269 · KPE

General Hospital · 42d

Medi-Plast Intl., Inc. - FDA 510(k) Cleared Devices

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