Medical Device Manufacturer · US , Iowa City , IA

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

9 submissions · 9 cleared · Since 1997

Total

Cleared

Denied

Protek Medical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Iowa City, US.

Historical record: 9 cleared submissions from 1997 to 1998. Primary specialty: Radiology.

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

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

9 devices

1-9 of 9

Cleared Jan 22, 1998

GENERAL PURPOSE ATL NEEDLE GUIDE KIT

K973958 · ITX

Radiology · 98d

Cleared Nov 26, 1997

TRANSDUCER POSITIONER

K973622 · ITX

Radiology · 64d

Cleared Oct 20, 1997

ULTRASOUND TRANSDUCER DRAPE

K970889 · KKX

General Hospital · 223d

Cleared Oct 20, 1997

ULTRASOUND TRANSDUCER DRAPE

K970893 · FYA

General Hospital · 223d

ULTRASOUND SYSTEMS DRAPE

K970885 · MMP

General Hospital · 195d

Cleared Aug 22, 1997

DRAPE, SURGICAL-LATEX

K970891 · KKX

General Hospital · 164d

Cleared Jul 10, 1997

TRANS VAGINAL NEEDLE GUIDE

K971722 · ITX

Radiology · 62d

Cleared Jun 13, 1997

GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE

K971115 · ITX

Radiology · 78d

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

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