FDA 510(k) Applications Submitted by TAUT, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960883 |
03/05/1996 |
INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8 |
TAUT, INC. |
| K972112 |
06/05/1997 |
INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450 |
TAUT, INC. |
| K962003 |
05/22/1996 |
TUAT SPLATTER CONTROL SHIELD SCS-300 |
TAUT, INC. |
| K021731 |
05/24/2002 |
ADAPT OPEN ACCESS PORT, MODEL 41233 |
TAUT, INC. |
| K023261 |
09/30/2002 |
ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244 |
TAUT, INC. |
| K011018 |
04/04/2001 |
TAUT BALLOON CATHETER, MODEL 50640 |
TAUT, INC. |
| K010007 |
01/02/2001 |
ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP |
TAUT, INC. |
| K992904 |
08/30/1999 |
MINI-PORT |
TAUT, INC. |
| K992907 |
08/30/1999 |
INTRADUCER |
TAUT, INC. |
| K003703 |
12/01/2000 |
TAUT-INSUFFLATION NEEDLE |
TAUT, INC. |
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