BK220699 - PUREGRAFT 50 SYSTEM
510(k) Number: BK220699
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 50 SYSTEM
Decision Date: 1/24/2014
510(k) Number: BK220699
Applicant: CYTORI THERAPEUTICS INC.
Device Name: PUREGRAFT 50 SYSTEM
Decision Date: 1/24/2014