Medical Device Manufacturer · US , Mchenry , IL

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

15 submissions · 15 cleared · Since 1979

Total

Cleared

Denied

Diatek, Inc. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1979 to 2002. Primary specialty: General Hospital.

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

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

15 devices

1-12 of 15

Cleared May 09, 2002

DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)

K020430 · NFK

Gastroenterology & Urology · 90d

Cleared Aug 14, 2001

DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC,...

K010399 · MSD

Gastroenterology & Urology · 186d

Cleared Dec 07, 1989

DIATEK MODEL 700 THERMOMETER

K895703 · FLL

General Hospital · 76d

Cleared Jan 27, 1988

MODIFICATION TO ARKIVE(TM)

K872178 · BSZ

Anesthesiology · 233d

Cleared Jan 12, 1987

ARKIVE (TM)

K862085 · BSZ

Anesthesiology · 224d

Cleared Jul 27, 1984

ENTEROPORT NUTRITION PUMP

K841827 · FRN

General Hospital · 85d

Cleared Jul 03, 1984

SECURA SET

K841859 · FPA

General Hospital · 60d

Cleared Jan 10, 1984

DIATEK 600 THERMOMETER SYSTEM

K833568 · FLL

General Hospital · 90d

Cleared Mar 09, 1983

SECURA SET SECONDARY ADMIN. SET

K830565 · FPA

General Hospital · 14d

Cleared Mar 01, 1983

SECURA IV VOLUMETRIC INFUSION PUMP

K830355 · FRN

General Hospital · 26d

Cleared Mar 01, 1983

SECURA SET PRIMARY ADMIN. SET

K830377 · FPA

General Hospital · 25d

Cleared Feb 25, 1983

SECURA SET VOLUME LIMITING SET

K830448 · FPA

General Hospital · 10d

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

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