Medical Device Manufacturer · US , Mchenry , IL

Clinipad Corp. - FDA 510(k) Cleared Devices

16 submissions · 12 cleared · Since 1980

Total

Cleared

Denied

Clinipad Corp. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1980 to 1994. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Clinipad Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Clinipad Corp.

16 devices

1-12 of 16

Cleared Jul 11, 1994

CARDIAC CATHETERIZATION TRAY

K931560 · DQO

Cardiovascular · 468d

Cleared Mar 07, 1994

PICC INSERTION TRAY

K931668 · FOZ

General Hospital · 335d

Cleared Feb 17, 1994

I.V. START KIT

K932071 · FOZ

General Hospital · 295d

Cleared Feb 03, 1994

V.A.D. ACCESS KIT

K932010 · LJT

General Hospital · 286d

Cleared Dec 13, 1993

LACERATION TRAY

K932036 · FRG

General Hospital · 230d

Cleared Nov 03, 1993

TRACHEOSTOMY CARE TRAY

K932016 · JOH

Anesthesiology · 194d

Cleared Oct 07, 1986

PUNCH BIOPSY KIT

K862562 · KNW

Gastroenterology & Urology · 96d

Cleared Jul 15, 1986

TRACHEOSTOMY CLEANSING SOLUTION

General & Plastic Surgery · 140d

Cleared Dec 28, 1983

CATHETER INSERTION KIT

K833432 · KOD

Gastroenterology & Urology · 84d

Cleared Mar 31, 1983

OR PREP KIT

K830476 · FRG

General Hospital · 44d

Cleared Mar 02, 1982

SUBCLAVIAN INSERTION KIT

K820171 · FRG

General Hospital · 40d

Clinipad Corp. - FDA 510(k) Cleared Devices

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