Medical Device Manufacturer · US , Mchenry , IL

J.S. Medical Assoc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1983

Total

Cleared

Denied

J.S. Medical Assoc. has 18 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 18 cleared submissions from 1983 to 1993.

Browse the FDA 510(k) cleared devices submitted by J.S. Medical Assoc. Filter by specialty or product code using the sidebar.

J.S. Medical Assoc. 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 - J.S. Medical Assoc.

18 devices

1-12 of 18

ACCUTEX IM LATEX TEST

K932551 · KTN

Immunology · 75d

Cleared Jul 28, 1993

ACCUTEX BETA-HCG TEST

K926112 · JHJ

Chemistry · 237d

Cleared Dec 07, 1992

ACCUTEX ASO LATEX TEST

K924247 · GTQ

Microbiology · 105d

Cleared Dec 07, 1992

ACCUTEX CRP LATEX TEST

K924332 · DCK

Immunology · 102d

Cleared Dec 01, 1992

ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST

ACCUTEX SLE LATEX TEST

J.S. Medical Assoc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - J.S. Medical Assoc.

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