PMA · Approved
ApprovedCybertach (TM) 60 Pulse Generator & Programmer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Boston Scientific · LWW Pulse-Generator, Single Chamber, Single
Approved on Nov 7, 1984 through premarket approval, which rests on the device’s own clinical evidence after a 945-day review.
- Decided
- Nov 7, 1984
- Review
- 945 days
- Class
- Class III
- Product code
- LWW
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P820022 has 5 supplements since 1985: changes to the approved device, its labelling or its manufacturing, each approved separately.
PMA supplements approved per year
View FIG. 1 as a table
| Year | Supplements approved |
|---|---|
| 1985 | 1 |
| 1990 | 1 |
| 2004 | 2 |
| 2012 | 1 |
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LWW? 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
Does it have a predicate?
PMA decisions do not claim a predicate device.
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.
How does its category compare?
All LWW devicesLWW Pulse-Generator, Single Chamber, Single: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LWW
2in 2012
2026 to Oct 25, outlined.
Median 510(k) review, days · LWW
Too few LWW 510(k)s in any year since 2007 to give a median.
Recalls per year · LWW
No recall names LWW since 2007.
Adverse event reports per year · LWW
2in 2024
MAUDE reports naming product code LWW, 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 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 2 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 2 |
| 2018 | 0 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 3 |
| 2020 | 0 | — | 0 | 2 |
| 2021 | 0 | — | 0 | 2 |
| 2022 | 0 | — | 0 | 2 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/P820022 · printed Nov 6, 2026
Cite this page
510(k) Report. “P820022: Cybertach (TM) 60 Pulse Generator & Programmer.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P820022
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026