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FDA 510(k) Applications Submitted by 9TH WAVE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
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.
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