Medical Device Manufacturer · US , Mchenry , IL

Earl-Clay Laboratories, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1984

Total

Cleared

Denied

Earl-Clay Laboratories, Inc. has 21 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1984 to 1986.

Browse the FDA 510(k) cleared devices submitted by Earl-Clay Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Earl-Clay Laboratories, Inc.

21 devices

1-12 of 21

Cleared May 13, 1986

ULTRACLONE 01-2300 CELL LINE

K861585 · KIR

Pathology · 14d

Cleared May 05, 1986

ULTRACLONE 01-700 CELL LINE

K861569 · KIR

Pathology · 7d

Cleared Oct 31, 1985

ULTRACLONE 05-100 GUINEA PIG RBC

K854206 · KPO

Pathology · 15d

Cleared Aug 12, 1985

ULTRACLONE ECL-01-2200 CELL LINE

K853203 · KIR

Pathology · 13d

Cleared May 10, 1985

ULTRACLONE ECL-01-800 CELL LINE

K851545 · KIR

Pathology · 24d

Cleared Oct 31, 1984

ULTRAXLONE ECL-01-1000 CELL LINE

K843577 · KIR

Hematology · 50d

Cleared Oct 31, 1984

ULTRACLONE ECL-01-2100 CELL LINE

K843578 · KIR

Hematology · 50d

Cleared Oct 31, 1984

ULTRACLONE ECL-01-1100

K843579 · KIR

Hematology · 50d

Cleared Oct 17, 1984

ULTRACLONE ECL-01-900 CELL LINE

K843862 · KIT

Pathology · 15d

Cleared Oct 17, 1984

ULTRACLONE ECL-01-1300 CELL LINE

K843863 · KIT

Pathology · 15d

Cleared Oct 17, 1984

ULTRACLONE ECL-01-1400 CELL LINE

K843864 · KIT

Pathology · 15d

Cleared May 11, 1984

ULTRACLONE ECL-01-800 CELL LINE

K841337 · KIR

Hematology · 39d

Earl-Clay Laboratories, Inc. - FDA 510(k) Cleared Devices

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