Medical Device Manufacturer · US , Mchenry , IL

Toa Medical Electronics USA, Inc. - FDA 510(k) Cleared Devices

33 submissions · 33 cleared · Since 1978

Recent clearances: SYSMEX SE-9000 AUTOMATED HEMATOLOGY ANALYZER, TOA MEDICAL ELECTRONICS CA-5000, CA-1000 AUTOMATED COAGULATION ANALYZER

Total

Cleared

Denied

Toa Medical Electronics USA, Inc. has 33 FDA 510(k) cleared hematology devices. Based in Mchenry, US.

Historical record: 33 cleared submissions from 1978 to 1994.

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

Toa Medical Electronics USA, Inc. is one of 13330 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Toa Medical Electronics USA, Inc.

33 devices

1-12 of 33

Cleared May 02, 1994

SYSMEX SE-9000 AUTOMATED HEMATOLOGY ANALYZER

K936023 · GKZ

Hematology · 138d

Cleared Jan 27, 1994

TOA MEDICAL ELECTRONICS CA-5000

K933886 · JPA

Hematology · 170d

Cleared Nov 03, 1993

CA-1000 AUTOMATED COAGULATION ANALYZER

K931149 · JPA

Hematology · 240d

Cleared Apr 29, 1992

SYSMEX HEMATOLOGY SYSTEM ACCESSORIES

K920544 · GKZ

Hematology · 83d

Cleared Dec 30, 1991

SYSMEX NE-1500, MODIFICATION

K914744 · GKZ

Hematology · 69d

Cleared Sep 10, 1991

SYSMEX(TM) R-3000 AUTOMATED RETICULOCYTE ANALYZER

SYSMEX R-1000 AUTOMATED RETICULOCYTE ANALYZER

Toa Medical Electronics USA, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Toa Medical Electronics USA, Inc.

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