FDA 510(k) Applications Submitted by JEAN ROZINT

FDA 510(k) Number Submission Date Device Name Applicant
K970081 01/09/1997 SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEM CATHAY CONSOLIDATED, INC.
K970364 01/31/1997 AIRTEC2 LOW AIR LOSS THERAPY BED APEX METAL, INC.
K972153 06/09/1997 ALTERNATING PRESSURE AIR FLOTATION MATTRESS DECUBITI CONCEPTS, INC.
K963620 09/10/1996 9TH WAVE MODELS 500 & 550 LOW AIR LOSS SYSTEMS 9TH WAVE, INC.
K963626 09/11/1996 9TH WAVE MODELS 400 & 450 ALTERNATING PRESSURE MATTRESS 9TH WAVE, INC.
K963677 09/13/1996 9TH WAVE MODEL 200 ALTERNATING PRESSURE PAD 9TH WAVE, INC.
K003909 12/19/2000 PROACT 1 PROACT CO.


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