510(k) K242225 ยท NLH Catheter, Recording, Electrode, Reprocessed
Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter
| Applicant | Surgical Instrument Service and Savings, Inc., Redmond OR, US |
| Decision | Substantially Equivalent, Nov 29, 2024 |
| Received | Jul 29, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242225
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 6, 2026 | Medline Industries, LP Reprocessed Abbott Inquiry Steerable Diagnostic Catheters:
Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm
81105RH
81172RH;
Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10- Open, Classified |
NLH | None listed |
| Sep 26, 2025 | Medline Industries, LP Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH Open, Classified |
NLH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.