P.T. Latexindo Tobaperkasa

P.T. Latexindo Tobaperkasa — FDA 510(k) Submissions

P.T. Latexindo Tobaperkasa has submitted 3 FDA 510(k) premarket notifications since 1997, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Latex Patient Examination Glove, Prosthesis, Hip, Hemi-, Femoral, Metal Ball, Vinyl Patient Examination Glove . Use the specialty filter in the sidebar to narrow results.