Taut, Inc.
Geneva, IL, US
Taut, Inc. appears in FDA device records in Geneva, IL. FDA records list 15 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Taut, Inc. between 1988 and 2002. The busiest year on record is 2001, with 3. The most recent is 2002, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1992 | 2 |
| 1993 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| 1997 | 1 |
| 1999 | 2 |
| 2001 | 3 |
| 2002 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023261 | ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244 | GCJ | Substantially Equivalent | |
| K021731 | ADAPT OPEN ACCESS PORT, MODEL 41233 | GCJ | Substantially Equivalent | |
| K011018 | TAUT BALLOON CATHETER, MODEL 50640 | GCA | Substantially Equivalent | |
| K010007 | ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP | GCJ | Substantially Equivalent | |
| K003703 | TAUT-INSUFFLATION NEEDLE | HIF | Substantially Equivalent | |
| K992907 | INTRADUCER | GBW | Substantially Equivalent | |
| K992904 | MINI-PORT | GBW | Substantially Equivalent | |
| K972112 | INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450 | GBW | Substantially Equivalent | |
| K962003 | TUAT SPLATTER CONTROL SHIELD SCS-300 | KKX | Substantially Equivalent | |
| K960883 | INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8 | GCJ | Substantially Equivalent | |
| K945486 | SPLATTER CONTROL SHIELD | KKX | Substantially Equivalent | |
| K924981 | OPERATIVE CHOLANGIOGRAM CATHETER | GBZ | Substantially Equivalent | |
| K921934 | INTRADUCER | GBX | Substantially Equivalent | |
| K920040 | INTRADUCER | GCJ | Substantially Equivalent | |
| K875082 | O.P.C. INTRAVASCULAR CATHETER | FOZ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GCABiliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection
- GBZCatheter, Cholangiography
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- GBXCatheter, Irrigation
- GBWCatheter, Peritoneal
- KKXDrape, Surgical, Antimicrobial
- HIFInsufflator, Laparoscopic
- GCJLaparoscope, General & Plastic Surgery
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain