FDA 510(k) Applications Submitted by Stan Yang
| 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. |
| K090612 |
03/06/2009 |
BENACEL |
UNICARE BIOMEDICAL |
| 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. |
| K982699 |
08/03/1998 |
UNIGRAFE |
UNICARE BIOMEDICAL |
| K092567 |
08/20/2009 |
MODIFICATION TO UNIGRAFT |
UNICARE BIOMEDICAL, INC. |
| K003457 |
11/07/2000 |
UNIGRAFT |
UNICARE BIOMEDICAL |
| K993784 |
11/08/1999 |
UNIGRAFT |
UNICARE BIOMEDICAL |
|
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