510(k) · Cleared
ClearedInspire SVR 1200, Inspire 6F C, Inspire 8F C
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sorin Group Italia S.R.L. · DTN Reservoir, Blood, Cardiopulmonary Bypass
Cleared on Mar 8, 2017 as substantially equivalent to K112771 (Sorin Group Italia S.R.L., 2011) after a 258-day review. Its family tree reaches back 3 generations to 1998.
- Decided
- Mar 8, 2017
- Review
- 258 days
- Class
- Class II
- Product code
- DTN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K980786 (1998). No later device cites it as a predicate yet.
- Root · 3 generations backK980786 Cobe Closed Venous Reservoir Bags with Smarx T, Models VRB 1200 and…Cobe Cardiovascular, Inc. · 1998
- 2 generations backK050111 Smarxt BMR 1900 Closed Venous Reservoir BagCobe Cardiovascular, Inc. · 2005
- 1 generation backK112771 BMR1900 PH.I.S.I.O Venous Reservoir BagSorin Group Italia S.R.L. · 2011
- This deviceK161733 Inspire SVR 1200, Inspire 6F C, Inspire 8F CSorin Group Italia S.R.L. · 2017
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K980786 | Cobe Closed Venous Reservoir Bags with Smarx T, Models VRB 1200 and VRB 1800 | Cobe Cardiovascular, Inc. | 1998 | — |
| −2 | K050111 | Smarxt BMR 1900 Closed Venous Reservoir Bag | Cobe Cardiovascular, Inc. | 2005 | — |
| −1 | K112771 | BMR1900 PH.I.S.I.O Venous Reservoir Bag | Sorin Group Italia S.R.L. | 2011 | — |
| 0 (this device) | K161733 | Inspire SVR 1200, Inspire 6F C, Inspire 8F C | Sorin Group Italia S.R.L. | 2017 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in DTN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new DTN device
- #1 K251783 Inspire HCR and HCR DUAL cardiotomy reservoirsscore 12.4 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K112771 | BMR1900 PH.I.S.I.O Venous Reservoir BagSummary page 4…monary Bypass Blood Reservoir (21 CFR 870.4400, Product Code DTN) PREDICATE DEVICE: BMR 1900 Ph.I.S.I.O.Venous Reservoir Bag (K112771) REFERENCE DEVICE: CBMVR800 Venous Reservoir Bag (K920774) DEVICE DESCRIPTION: The Sorin INSPIRE SVR 1200 (hereina… | 2011 |
| † | K920774 | MVR Collapsible Venous Reservoir Bag | 1992 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 19 years and passes through 2 companies; a new generation was cleared every 6.5 years on median.
- None of the 3 ancestors has a recall.
- 1 other device also cites its predicate K112771.
How does its category compare?
All DTN devicesDTN Reservoir, Blood, Cardiopulmonary Bypass: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · DTN
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DTN
38in 2014
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DTN
2in 2018
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DTN
8in 2025
MAUDE reports naming product code DTN, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 1 | 10 |
| 2008 | 1 | — | 1 | 8 |
| 2009 | 7 | 211 | 1 | 10 |
| 2010 | 1 | — | 0 | 18 |
| 2011 | 2 | — | 1 | 10 |
| 2012 | 0 | — | 0 | 17 |
| 2013 | 4 | 79 | 0 | 47 |
| 2014 | 3 | 38 | 0 | 52 |
| 2015 | 2 | — | 0 | 27 |
| 2016 | 0 | — | 1 | 6 |
| 2017 | 2 | — | 1 | 3 |
| 2018 | 0 | — | 2 | 4 |
| 2019 | 0 | — | 0 | 11 |
| 2020 | 0 | — | 0 | 6 |
| 2021 | 0 | — | 0 | 12 |
| 2022 | 0 | — | 0 | 7 |
| 2023 | 1 | — | 0 | 8 |
| 2024 | 2 | — | 0 | 10 |
| 2025 | 1 | — | 0 | 8 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
INSPIRE SVR 1200 with Ph.I.S.I.O. coating is intended for use in adult and small adult surgical procedures requiring cardiopulmonary bypass. It collects and handles venous blood and suction blood from cardiotomy reservoir. The INSPIRE SVR 1200 is intended to be used for 6 hours or less.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K161733 · printed Nov 6, 2026
Cite this page
510(k) Report. “K161733: Inspire SVR 1200, Inspire 6F C, Inspire 8F C.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K161733
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026