Medical Device Manufacturer · US , Mchenry , IL

Verimed Holdings, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1983

Total

Cleared

Denied

Verimed Holdings, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1983 to 1998. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Verimed Holdings, Inc. Filter by specialty or product code using the sidebar.

Verimed Holdings, 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 - Verimed Holdings, Inc.

12 devices

1-12 of 12

Cleared Nov 20, 1998

PERIFORM

K981277 · HIR

Gastroenterology & Urology · 226d

Physical Medicine · 143d

Cleared Dec 10, 1992

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)

Gastroenterology & Urology · 292d

Cleared Mar 07, 1990

VERIMED MYOEXORCISER VERISTIM

K893220 · IPF

Physical Medicine · 314d

Cleared Dec 13, 1989

VERIMED MYOEXORCISER III (MYO III)

Physical Medicine · 297d

Cleared Jun 09, 1986

ELECTRO-MYOGRAPHIC PERINEOMETER

K854193 · HIR

Gastroenterology & Urology · 237d

Verimed Holdings, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Verimed Holdings, Inc.

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