FDA 510(k) Applications Submitted by BARBARA ATZENHOEFER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960406 |
01/29/1996 |
BRAUN HEMOSTASIS INTRODUCERS |
B. BRAUN MEDICAL, INC. |
| K971048 |
03/21/1997 |
PERI-STRIPS DRY - STAPLE LINE REINFORCEMENT |
BIO-VASCULAR, INC. |
| K971726 |
05/09/1997 |
CV PERI-GUARD - CARDIOVASCULAR PATCH |
BIO-VASCULAR, INC. |
| K973706 |
09/29/1997 |
DURA-GUARD-DURAL REPAIR PATCH |
BIO-VASCULAR, INC. |
| K955485 |
12/01/1995 |
BRUN SELECTIVE AND FLUSH ANGIOGRAPHIC CATHETERS |
B. BRAUN MEDICAL, INC. |
| K955820 |
12/26/1995 |
BRAUN HEMOSTASIS INTRODUCERS |
B. BRAUN MEDICAL, INC. |
| K100305 |
02/03/2010 |
ETURN SPINAL IMPLANT MODEL ETURN XX-12; ETURN XX-16 WHERE XX=07, 09, 11, 13, OR 15 AND ETURN XX-12 K; ETURN XX-16 K WHER |
ICOTEC |
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