Medical Device Manufacturer · US , Mchenry , IL

Lancer Assoc.

2 submissions · 2 cleared · Since 1983

Total

Cleared

Denied

Lancer Assoc. — FDA 510(k) Submissions

Lancer Assoc. has submitted 2 FDA 510(k) premarket notifications since 1983, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Exerciser, Non-measuring, Device, Patient Transfer, Powered . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

TENDER LIFTING CARE

K840796 · FRZ Device, Patient Transfer,... · General Hospital

Apr 1984 57d

GIREX

K831033 · ION Exerciser, Non-measuring · Physical Medicine

Apr 1983 27d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Lancer Assoc.

Lancer Assoc. — FDA 510(k) Submissions

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