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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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