Medical Device Manufacturer · US , Mchenry , IL

Laprol Scientific, Inc.

3 submissions · 3 cleared · Since 1983
3
Total
3
Cleared
0
Denied

Laprol Scientific, Inc. — FDA 510(k) Submissions

Laprol Scientific, Inc. has submitted 3 FDA 510(k) premarket notifications since 1983, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Acid, Ascorbic, 2,4-dinitrophenylhydrazine (spectrophotometric), Method, Enzymatic, Glucose (urinary, Non-quantitative), Nitroprusside, Ketones (urinary, Non-quant.) . Use the specialty filter in the sidebar to narrow results.

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