Medical Device Manufacturer · US , Portland , OR

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

29 submissions · 29 cleared · Since 1990

Total

Cleared

Denied

Crestat Diagnostics, Inc. has 29 FDA 510(k) cleared medical devices. Based in Portland, US.

Historical record: 29 cleared submissions from 1990 to 1998. Primary specialty: Immunology.

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

Crestat Diagnostics, 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 - Crestat Diagnostics, Inc.

29 devices

1-12 of 29

N-ASSAY TIA PLASMINOGEN TEST KIT

K971985 · GGP

Hematology · 144d

Cleared Oct 20, 1997

N-ASSAY TIA ANTITHROMBIN III TEST KIT

K972257 · DDQ

Hematology · 125d

Cleared Aug 01, 1997

N-ASSAY TIA APO A1 TEST KIT

K964292 · DER

Immunology · 276d

Cleared Aug 01, 1997

N-ASSAY TIA APO A1/B MULTI CALIBRATOR

K964294 · DER

Immunology · 276d

Cleared Aug 01, 1997

N-ASSAY TIA APO B TEST KIT

K964296 · DER

Immunology · 276d

Cleared Jul 14, 1997

N-ASSAY TIA C4 TEST KIT

K964297 · DBI

Immunology · 258d

Cleared Jul 14, 1997

N-ASSAY TIA MULTI V-NL

K964298 · CZW

Immunology · 258d

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

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

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