Medical Device Manufacturer · US , Grand Rapids , MI

Mar-Med Co.

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Mar-Med Co. — FDA 510(k) Submissions

Mar-Med Co. has submitted 1 FDA 510(k) premarket notifications since 1993, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Clamp, Surgical, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

MAR-MED LIVER STRAP

K924223 · GDJ Clamp, Surgical, General... · General & Plastic Surgery

Mar 1993 209d

Mar-Med Co.

Mar-Med Co. — FDA 510(k) Submissions

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