Medical Device Manufacturer · US , Washington , DC

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

24 submissions · 24 cleared · Since 1985

Total

Cleared

Denied

Mediatech, Inc. has 24 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 24 cleared submissions from 1985 to 1986. Primary specialty: Microbiology.

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

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

24 devices

1-12 of 24

Cleared Mar 03, 1986

CELLGRO HEPES BUFFER SOLUTION

K860623 · KIT

Pathology · 12d

Cleared Dec 06, 1985

PENICILLIN/STREPTOMYCIN SOLUTION

K854567 · KIT

Pathology · 22d

Cleared Jul 12, 1985

CELLGRO WILLIAMS' MEDIUM E

K852475 · KIT

Pathology · 31d

Cleared Jul 12, 1985

CELLGRO(ISCOVE'S MEDIUM) MODIFICATION

K852485 · KIT

Pathology · 31d

Cleared Jul 12, 1985

MCCOY'S 5A MEDIUM-LIQUID FORM

K852602 · KIT

Pathology · 23d

Cleared Jul 12, 1985

MCCOY'S 5A MEDIUM - POWDERED FORM

EMEM W/NEAA-MINIMUM ESSENTIAL MED. W/NON-ESS. AMIN

K850510 · KIT

Microbiology · 24d

Cleared Feb 27, 1985

EMEM-EARLE'S MINIMUM ESSENTIAL MED. W/GLUTAMINE-EA

K850511 · KIT

Pathology · 19d

Cleared Feb 27, 1985

DMEM-DULBECCO'S MINIMUM ESSENTIAL MEDIUM

K850512 · KIT

Pathology · 19d

Cleared Feb 27, 1985

RPMI 1640-ROSWELL PARK MEMORIAL INSTITUTE 1640

K850513 · KIT

Microbiology · 19d

Cleared Feb 27, 1985

ALPHA MEM-ALPHA MINIMUM ESSENTIAL MED. W/O RIBOSID

K850514 · KIT

Microbiology · 19d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026

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

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