Medical Device Manufacturer · US , Mchenry , IL

Procedure Products, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1981

Total

Cleared

Denied

Procedure Products, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1981 to 2017. Primary specialty: General Hospital.

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

Procedure Products, Inc. is one of 4728 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Procedure Products, Inc.

16 devices

1-12 of 16

Cleared Mar 27, 2017

Freedom Syringe

K161812 · FMF

General Hospital · 269d

Cleared Oct 08, 1993

INSUFFLATOR CONNECTING FILTER

K923194 · HIF

Obstetrics & Gynecology · 465d

Cleared Dec 10, 1992

TORQUE DEVICE

K922536 · DQX

Cardiovascular · 196d

General Hospital · 68d

Cleared Dec 20, 1988

MODIFIED 10CC SYRINGE CONTROL RING SET

K884985 · FMF

General Hospital · 19d

Cleared Feb 04, 1988

10CC SYRINGE CONTROL RING SET

K874747 · FMF

General Hospital · 78d

Cleared Jan 29, 1988

ANGIO WASTE FLUIDS DUMP BAG

K874037 · DQO

Cardiovascular · 116d

Cleared Jan 13, 1986

CUSTOM CORONARY MANIFOLD KITS

K853749 · DTL

Cardiovascular · 126d

Cleared Sep 05, 1984

DISPOSABLE STOPCOCKS

K842173 · FMG

General Hospital · 113d

Cleared Mar 12, 1984

MATERIAL ADDITION LEXAN & K-RESIN

K833554 · DQO

Cardiovascular · 159d

Cleared Apr 15, 1982

GLASS SYRINGES, DRUG, LUER LOCK

K820384 · FMF

General Hospital · 65d

Procedure Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Procedure Products, Inc.

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