Tandem T: Slim Autosoft XC Kit
AutoSoft XC, 23"/6 mm 10 Pack
1manufacturer
2catalogue numbers in this listing
6510(k) clearances naming this product code
Who Else Makes It
Registered in Jiangsu.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Steris Sterilization Technologies (Suzhou) Ltd | Suzhou | Jiangsu | Contract manufacturer | 44 |
Record
| Listed by | Tandem Diabetes Care, Inc., United States |
|---|---|
| FDA product code | QJI |
| Device type | Interoperable Automated Glycemic Controller |
| Device class | Class 2 |
| Regulation | 21 CFR 862.1356 |
| Establishment | Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K232380 |
| Record published | 2025-12-12 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1018587 | In distribution | |
| 1018575 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| twiist | Sequel MED Tech, LLC | 8 |
| iLet Bionic Pancreas | Beta Bionics, Inc. | 6 |
| Tandem t:slim Autosoft 30 Kit | Tandem Diabetes Care, Inc. | 4 |
| iLet Starter Kit – Inset 23″ | Beta Bionics, Inc. | 1 |
| iLet Starter Kit | Beta Bionics, Inc. | 1 |
| t:slim X2 Insulin Pump with Control-IQ | Tandem Diabetes Care, Inc. | 1 |
| iLet Starter Kit – Contact Detach | Beta Bionics, Inc. | 1 |
| Tandem t:slimTruSteel Kit | Tandem Diabetes Care, Inc. | 1 |
| iLet Starter Kit – Inset 32″ | Beta Bionics, Inc. | 1 |
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K260429 | 2026-04-24 |
| K250798 | 2025-05-21 |
| K243823 | 2025-02-24 |
| K232382 | 2023-11-03 |
| K200467 | 2020-06-16 |
| DEN190034 | 2019-12-13 |
Recalls Naming This Product
3 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Tandem Diabetes Care, Inc. | 510(k) number | 2026-01-30 | Class II | Process change control | The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confir | 1,380 units |
| Tandem Diabetes Care, Inc. | 510(k) number | 2025-07-03 | Class II | Software design | an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or hyperglycemia. | 19 |
| Tandem Diabetes Care, Inc. | 510(k) number | 2025-02-27 | Class I | Software Design Change | A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is | 63 units |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.