FDA 510(k) Applications Submitted by ALAIN DUPRAT

FDA 510(k) Number Submission Date Device Name Applicant
K960395 01/29/1996 PLANCON MIRCOLAMELLAR KERATOME PLANCON INSTRUMENTS
K970377 02/03/1997 PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES) PLANCON INSTRUMENTS
K980924 03/11/1998 PLANCON MICROLAMELLAR KERATOME EVOLUTION PLANCON INSTRUMENTS
K981741 05/18/1998 CARRIAZO BARRAQUER MICROKERATOME MORIA, INC.
K981742 05/18/1998 ONE UP DISPOSABLE KERATOME HEAD MORIA, INC.


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