Medical Device Manufacturer · US , Walker , MI

Meridian Diagnostics, Inc. - FDA 510(k) Cleared Devices

92 submissions · 92 cleared · Since 1980

Total

Cleared

Denied

Meridian Diagnostics, Inc. has 92 FDA 510(k) cleared microbiology devices. Based in Walker, US.

Historical record: 92 cleared submissions from 1980 to 1999.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Meridian Diagnostics, Inc.

92 devices

1-12 of 92

Cleared Dec 10, 1999

PREMIER TOXINS A&B, MODEL 616096

K993914 · LLH

Microbiology · 23d

Cleared Aug 09, 1999

IMMUNOCARD STAT! E. COLI O157:H7

K990263 · GMZ

Microbiology · 194d

Cleared Jun 25, 1999

PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST

K984343 · MXJ

Microbiology · 203d

Cleared Jun 25, 1999

PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST

K984346 · LGC

Microbiology · 203d

Cleared Dec 17, 1998

MODIFICATION TO: PREMIER PLATINUM HPSA

K983255 · LYR

Microbiology · 93d

Cleared Dec 03, 1998

PREMIER CRYPTOSPORIDIUM

PREMIER PLATINUM HPSA

IMMUNOCARD STAT! ROTAVIRUS

Looking for a specific device from Meridian Diagnostics, Inc.? Search by device name or K-number.

Search all Meridian Diagnostics,... devices

Meridian Diagnostics, Inc. - FDA 510(k) Cleared Devices

Filters