BK220693 - PUREGRAFT 850/PURE SYSTEM
510(k) Number: BK220693
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 850/PURE SYSTEM
Decision Date: 3/7/2012
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510(k) Number: BK220693
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 850/PURE SYSTEM
Decision Date: 3/7/2012