510(k) · Cleared
ClearedReprocessed BRK Transseptal Needle
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Innovative Health, LLC · NMK Trocar, Reprocessed
Cleared on Jul 22, 2020 as substantially equivalent to K122587 (St Jude Medical, 2013) and 1 other predicate after a 268-day review. Its family tree reaches back 6 generations to 1997.
- Decided
- Jul 22, 2020
- Review
- 268 days
- Class
- Class II
- Product code
- NMK
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 6 generations to K964518 (1997). 8 ancestors in all. No later device cites it as a predicate yet.
- Root · 6 generations backK964518 Fast-Cath Transseptal Catheter IntroducerDaig Corp. · 1997 · Recalled
- 5 generations backK042623 Agilis Steerable Catheter Introducer, Model 408304St. Jude Medical, Daig Division, Inc. · 2005 · Recalled
- 4 generations backK052644 Swartz Braided Transseptal Guiding IntroducerSt Jude Medical · 2005
- 3 generations backK070417 Across Transseptal Access System, 406977, 406978, 406979, 406980…St Jude Medical · 2007
- 2 generations backK072278 BRK Transseptal NeedleSt Jude Medical · 2007
- 1 generation backK122587 BRK Transseptal Needle Model 407200, 407201, 407205, 407206, 407207…St Jude Medical · 2013
- This deviceK192998 Reprocessed BRK Transseptal NeedleInnovative Health, LLC · 2020
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K964518 | Fast-Cath Transseptal Catheter Introducer | Daig Corp. | 1997 | 4 |
| −5 | K042623 | Agilis Steerable Catheter Introducer, Model 408304 | St. Jude Medical, Daig Division, Inc. | 2005 | 1 |
| −4 | K052644 | Swartz Braided Transseptal Guiding Introducer | St Jude Medical | 2005 | — |
| −3 | K070417 | Across Transseptal Access System, 406977, 406978, 406979, 406980, 406981… | St Jude Medical | 2007 | — |
| −2 | K072278 | BRK Transseptal Needle | St Jude Medical | 2007 | — |
| −1 | K122587 | BRK Transseptal Needle Model 407200, 407201, 407205, 407206, 407207, G407208 | St Jude Medical | 2013 | — |
| 0 (this device) | K192998 | Reprocessed BRK Transseptal Needle | Innovative Health, LLC | 2020 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
| 2002 | 1 | 0 |
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 NMK? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K122587 | BRK Transseptal Needle Model 407200, 407201, 407205, 407206, 407207, G407208Summary page 5…on Number: Class II, 21 CFR §870.1390 Product Code: NMK Predicate Device: 510(k) Number 510(k) Device Manufacturer K122587 BRK Transseptal Needle St. Jude Medical K072278 BRK Transseptal Needle St. Jude… | 2013 |
| * | K072278 | BRK Transseptal NeedleSummary page 5…NMK Predicate Device: 510(k) Number 510(k) Device Manufacturer K122587 BRK Transseptal Needle St. Jude Medical K072278 BRK Transseptal Needle St. Jude Medical Reference Device: 510(k) Number 510(k) Device… | 2007 |
| † | K172950 | TSN Transseptal Needle | 2018 |
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 23 years and passes through 4 companies; a new generation was cleared every 5.4 years on median.
- 4 of the 8 ancestors have a recall of any class.
- 3 other devices also cite its predicate K122587.
How does its category compare?
All NMK devicesNMK Trocar, Reprocessed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · NMK
1in 2020
2026 to Oct 25, outlined.
Median 510(k) review, days · NMK
Too few NMK 510(k)s in any year since 2007 to give a median.
Recalls per year · NMK
No recall names NMK since 2007.
Adverse event reports per year · NMK
1in 2025
MAUDE reports naming product code NMK, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 1 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 1 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 1 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Reprocessed BRK Transseptal Needle is used to puncture the interatrial septum during a transseptal catheterization procedure to gain left heart access.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K192998 · printed Nov 5, 2026
Cite this page
510(k) Report. “K192998: Reprocessed BRK Transseptal Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K192998
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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