Medical Device Manufacturer · US , Mchenry , IL

Pro-Lab, Inc. - FDA 510(k) Cleared Devices

27 submissions · 26 cleared · Since 1984

Total

Cleared

Denied

Pro-Lab, Inc. has 26 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 26 cleared submissions from 1984 to 1995. Primary specialty: Microbiology.

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

Pro-Lab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pro-Lab, Inc.

27 devices

1-12 of 27

Cleared Jan 27, 1995

PROLEX (STREPTOCCAL GROUPING LATEX KIT)

LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY

K921421 · LHL

Microbiology · 126d

Cleared Jan 24, 1991

E. COLI 0157 LATEX TEST

NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST

General & Plastic Surgery · 106d

Cleared Jun 03, 1986

HIPPURATE HYDROLYSIS TEST

Pro-Lab, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Pro-Lab, Inc.

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