Medical Device Manufacturer · US , Mchenry , IL

Dutchland Laboratories, Inc. - FDA 510(k) Cleared Devices

75 submissions · 75 cleared · Since 1981

Total

Cleared

Denied

Dutchland Laboratories, Inc. has 75 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 75 cleared submissions from 1981 to 1982. Primary specialty: Microbiology.

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

FDA 510(k) Regulatory Record - Dutchland Laboratories, Inc.

75 devices

1-12 of 75

Cleared Jul 27, 1982

S-MEM-JOKLIK'S POWDER

K821911 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

MCCOY'S POWDER MEDIUM 5A SUSPENSION

K821912 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

ISCOVE'S MODIFIED DULBECCO POWDER MEDIUM

K821913 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

COON'S F-12 POWDER MEDIUM

K821914 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

BME AUTOCLAVABLE MEDIUM

K821915 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

IMPROVED MEM-RICHTER'S POWDER MODIF.

K821916 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

WAYMOUTH'S POWDER MEDIUM

K821917 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

POWDERED RPMI-1603 MEDIUM

K821918 · KIT

Microbiology · 29d

Cleared Jul 27, 1982

POWDERED RPMI-1634 MEDIUM

MEM AUTOCLAVABLE MEDIUM

K820915 · KIT

Microbiology · 20d

Cleared Apr 21, 1982

D-MEM-HIGH GLUCOSE-POWDERED MEDIUM

K820916 · KIT

Microbiology · 20d

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Dutchland Laboratories, Inc. - FDA 510(k) Cleared Devices

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