FDA 510(k) Applications Submitted by Unicare Biomedical, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K090083 |
01/12/2009 |
CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090 |
UNICARE BIOMEDICAL, INC. |
K080532 |
02/26/2008 |
BENACEL, MODELS C-001, C-002 AND C-005 |
UNICARE BIOMEDICAL, INC. |
K020720 |
03/05/2002 |
OSSIFORM |
UNICARE BIOMEDICAL, INC. |
K021511 |
05/09/2002 |
CYTOFLEX MESH |
UNICARE BIOMEDICAL, INC. |
K151344 |
05/19/2015 |
Cytoflex Tefguard Ti-Enforced Membrane |
Unicare Biomedical, Inc. |
K012144 |
07/10/2001 |
CYTOFLEX |
UNICARE BIOMEDICAL, INC. |
K092567 |
08/20/2009 |
MODIFICATION TO UNIGRAFT |
UNICARE BIOMEDICAL, INC. |
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