Medical Device Manufacturer · US , Mchenry , IL

Dynatech Corp. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1979

Total

Cleared

Denied

Dynatech Corp. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 27 cleared submissions from 1979 to 1991. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Dynatech Corp. Filter by specialty or product code using the sidebar.

Dynatech Corp. 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 - Dynatech Corp.

27 devices

1-12 of 27

Cleared Jan 28, 1991

DYNATECH MR4000 MICROPLATE READER

IMMULON SUBSTRATE REMOVAWELL STRIPS

MICRO STIX #011-010-5000 & HOLDER#5100

K823833 · LIB

Chemistry · 77d

Cleared Feb 16, 1983

MICROELISA MINIREADER II

K830200 · LBI

Chemistry · 27d

Cleared Jan 21, 1983

PROVIAL II #006-010-0201

MICROFLUOR B PLATE & MICRO FLUOR W PLATE

K822960 · LIB

Chemistry · 42d

Cleared Nov 16, 1982

MICROFLUOR B REMOVAWELL STRIPS

K822962 · LIB

Chemistry · 42d

Dynatech Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Dynatech Corp.

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