Medical Device Manufacturer · US , Chester , NJ

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

10 submissions · 10 cleared · Since 1991

Total

Cleared

Denied

Cirrus Diagnostics, Inc. has 10 FDA 510(k) cleared chemistry devices. Based in Chester, US.

Historical record: 10 cleared submissions from 1991 to 1992.

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

Cirrus 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 - Cirrus Diagnostics, Inc.

10 devices

1-10 of 10

IMMULITE(TM) T-UPTAKE

K910677 · CEE

Chemistry · 73d

Cleared Apr 16, 1991

IMMULITE(TM) TOTAL T4

K910261 · KLI

Chemistry · 84d

Cleared Mar 06, 1991

CRP LIPID REAGENT TEST PACK

K905648 · CHH

Chemistry · 79d

Cleared Feb 01, 1991

IMMULITE (TM) TOTAL T3

IMMULITE (TM) AUTOMATED IMMUNOASSAY ANALYZER

K905215 · JJQ

Chemistry · 52d

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

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

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