Taut, Inc.
Taut, Inc. appears in FDA public data with 0 recalls, 16 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 13, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 16
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K023261 | ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244 | December 13, 2002 |
| K021731 | ADAPT OPEN ACCESS PORT, MODEL 41233 | August 8, 2002 |
| K011018 | TAUT BALLOON CATHETER, MODEL 50640 | June 22, 2001 |
| K010007 | ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP | February 22, 2001 |
| K003703 | TAUT-INSUFFLATION NEEDLE | February 22, 2001 |
| K992904 | MINI-PORT | October 5, 1999 |
| K992907 | INTRADUCER | October 5, 1999 |
| K972112 | INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450 | December 1, 1997 |
| K962003 | TUAT SPLATTER CONTROL SHIELD SCS-300 | July 18, 1996 |
| K960883 | INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8 | March 20, 1996 |
| K945486 | SPLATTER CONTROL SHIELD | February 28, 1995 |
| K924981 | OPERATIVE CHOLANGIOGRAM CATHETER | April 6, 1993 |
| K921934 | INTRADUCER | July 15, 1992 |
| K920040 | INTRADUCER | February 28, 1992 |
| K875082 | O.P.C. INTRAVASCULAR CATHETER | March 8, 1988 |
| K830573 | PRE VUE | March 29, 1983 |