Medical Device Manufacturer · US , Mchenry , IL

Alpha-Tec Systems, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1983

Total

Cleared

Denied

Alpha-Tec Systems, Inc. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1983 to 2006. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Alpha-Tec Systems, Inc. Filter by specialty or product code using the sidebar.

Alpha-Tec Systems, 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 - Alpha-Tec Systems, Inc.

18 devices

1-12 of 18

ATS DOBELL & O'CONNOR'S IODINE

K890861 · JTS

Pathology · 30d

Cleared Feb 24, 1989

ATS LUGOL'S IODINE SOLUTION

K890020 · JTS

Pathology · 51d

Cleared Jan 24, 1989

ATS TB RAPID STAIN SET PRODUCT #034-45

ATS PARA-SET MODIFIED PVA FIXATIVE SOLUTION

K883048 · LDZ

Pathology · 32d

Cleared Aug 17, 1988

ATS PARA-SET IODINE ALCOHOL SOLUTION

K883049 · JTS

Pathology · 29d

Cleared Aug 04, 1988

ATS SCHAUDINN'S FIXATIVE W/ACETIC ACID

ATS CRYPTOSPORIDIUM STAIN SET

K880989 · JTS

Pathology · 66d

Cleared May 13, 1988

ATS PVA FIXATIVE SOLUTION

K881698 · LDZ

Pathology · 24d

Cleared May 13, 1988

ATS M/15 PHOSPHATE BUFFER, PRODUCT #034-42

K881879 · JSK

Pathology · 9d

Alpha-Tec Systems, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Alpha-Tec Systems, Inc.

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