Medical Device Manufacturer · US , Denver , PA

Hazleton Research Products, Inc. - FDA 510(k) Cleared Devices

47 submissions · 47 cleared · Since 1985

Total

Cleared

Denied

Hazleton Research Products, Inc. has 47 FDA 510(k) cleared pathology devices. Based in Denver, US.

Historical record: 47 cleared submissions from 1985 to 1986.

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

FDA 510(k) Regulatory Record - Hazleton Research Products, Inc.

47 devices

1-12 of 47

Cleared Jun 10, 1986

PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE

K861997 · JSK

Microbiology · 18d

Cleared Jun 09, 1986

DULBECCO'S MEM WITH 4.5 G/L GLUCOSE MEDIUM

K861996 · KIT

Pathology · 17d

Cleared May 29, 1986

MEM ALPHA EAGLE MEDIUM

DULBECCO'S MODIFIED EAGLE MED. W/25MM HEPES BUFFER

ISCOVE'S (MODIFIED) DULBECCO'S MEDIUM

MINIMUM ESSENTIAL MED. (EAGLE) W/25MM HEPES BUFFER

K861874 · KIT

Pathology · 14d

Cleared May 29, 1986

RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER

K861875 · KIT

Pathology · 14d

Cleared May 29, 1986

WILLIAMS MEDIUM E POWDER

K861885 · KIT

Pathology · 13d

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Hazleton Research Products, Inc. - FDA 510(k) Cleared Devices

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