510(k) · Cleared
ClearedAlexander Manufacturing CO. Rechargeable Battery Part Number M212
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Alexander Mfg. Co. · FLN Monitor, Electric For Gravity Flow Infusion Systems
Cleared on Jul 3, 1997 as substantially equivalent to K844556 (The Timeter Group, 1985) after a 29-day review. Its family tree reaches back 1 generation to 1985.
- Decided
- Jul 3, 1997
- Review
- 29 days
- Class
- Class II
- Product code
- FLN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K844556 (1985). No later device cites it as a predicate yet.
- Root · 1 generation backK844556 KHM 2000 Drip WatcherThe Timeter Group · 1985
- This deviceK972084 Alexander Manufacturing CO. Rechargeable Battery Part Number M212Alexander Mfg. Co. · 1997
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K844556 | KHM 2000 Drip Watcher | The Timeter Group | 1985 | — |
| 0 (this device) | K972084 | Alexander Manufacturing CO. Rechargeable Battery Part Number M212 | Alexander Mfg. Co. | 1997 | — |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FLN? 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? (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 |
|---|---|---|---|
| * | K844556 | KHM 2000 Drip WatcherSummary page 3…510(k) Number: (\‘H ld%lf Device Name: ~"M212 " - Indications for Use: Replacement battery for Timeter 41B905FD19G1 KHM2000 Drip Watcher Monitor Insert, 510(k) Number K844556. This battery is shipped only to customers who request a replacement battery for a particular device or to replace a competitor’… | 1985 |
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?
- Its one ancestor has no recall.
How does its category compare?
All FLN devicesFLN Monitor, Electric For Gravity Flow Infusion Systems: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FLN
1in 2018
2026 to Oct 25, outlined.
Median 510(k) review, days · FLN
Too few FLN 510(k)s in any year since 2007 to give a median.
Recalls per year · FLN
No recall names FLN since 2007.
Adverse event reports per year · FLN
2in 2025
MAUDE reports naming product code FLN, 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 | 1 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 1 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 1 |
| 2018 | 1 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 2 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 2 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Replacement battery for Timeter 41B905FD19G1 KHM2000 Drip Watcher Monitor Insert, 510(k) Number K844556.
This battery is shipped only to customers who request a replacement battery for a particular device or to replace a competitor’s replacement battery. The biomedical equipment technician therefore knows the intended use is as a replacement battery.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K972084 · printed Nov 6, 2026
Cite this page
510(k) Report. “K972084: Alexander Manufacturing CO. Rechargeable Battery Part Number M212.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K972084
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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