510(k) · Cleared
Recalled · Class II · 2021Moblvac Iii
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Aeros Instruments, Inc. · BTA Pump, Portable, Aspiration (Manual Or Powered)
Cleared on May 20, 1994 after a 283-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 94 later devices descend from it. It has been recalled once.
- Decided
- May 20, 1994
- Review
- 283 days
- Class
- Class II
- Product code
- BTA
- Recalls
- 1
- Predicates
- 0
94 later devices descend from it, 1 citing it directly.
- This deviceK933902 Moblvac IiiAeros Instruments, Inc. · 1994
- Descendant · cites it directly · 93 of its ownK043544 Medela Dominant 35 C/I Secretion and Surgical AspiratorMedela AG · 2005
- Descendant · 2 generations on · 85 of its ownK061205 Medela Vario 8/18/CI Secretion & Surgical AspiratorMedela AG · 2006 · Recalled
- Descendant · 3 generations on · 75 of its ownK080357 Medela Invia Wound TherapyMedela AG · 2008 · Recalled
- Descendant · 4 generations on · 56 of its ownK083375 Renasys GO Negative Pressure Wound TherapySmith & Nephew, Inc. · 2009 · Recalled
- Descendant · 5 generations on · 26 of its ownK111170 PICOSmith & Nephew, Inc. · 2011
Showing 5 of 94 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 94 · See all- K043544Medela Dominant 35 C/I Secretion and Surgical AspiratorMedela AG · 2005 · cites it directly93descendants
- K061205Medela Vario 8/18/CI Secretion & Surgical AspiratorMedela AG · 2006 · 2 generations on85descendants
- K080357Medela Invia Wound TherapyMedela AG · 2008 · 3 generations on75descendants
- K083375Renasys GO Negative Pressure Wound TherapySmith & Nephew, Inc. · 2009 · 4 generations on56descendants
- K111170PICOSmith & Nephew, Inc. · 2011 · 5 generations on26descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K933902 | Moblvac Iii | Aeros Instruments, Inc. | 1994 | — |
| +1 | K043544 | Medela Dominant 35 C/I Secretion and Surgical Aspirator | Medela AG | 2005 | — |
| +2 | K061205 | Medela Vario 8/18/CI Secretion & Surgical Aspirator | Medela AG | 2006 | 1 |
| +3 | K080357 | Medela Invia Wound Therapy | Medela AG | 2008 | 1 |
| +4 | K083375 | Renasys GO Negative Pressure Wound Therapy | Smith & Nephew, Inc. | 2009 | 2 |
| +5 | K111170 | PICO | Smith & Nephew, Inc. | 2011 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 3 | 0 |
| 2012 | 6 | 0 |
| 2013 | 2 | 0 |
| 2014 | 6 | 0 |
| 2015 | 5 | 0 |
| 2016 | 11 | 0 |
| 2017 | 8 | 0 |
| 2018 | 10 | 0 |
| 2019 | 8 | 0 |
| 2020 | 4 | 0 |
| 2021 | 3 | 0 |
| 2022 | 9 | 0 |
| 2023 | 3 | 0 |
| 2024 | 2 | 0 |
| 2025 | 4 | 0 |
| 2026 | 3 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in BTA? 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 BTA device
- #1 K222547 Electric nasal aspiratorscore 20.7 · 6 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
What descends from it? (94)
See all 941 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K043544 | Medela Dominant 35 C/I Secretion and Surgical Aspirator | 2005 | 93 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Nov 16, 2021 | Class II | Z-0482-2022 | Employee error | Increase in premature device failures |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K043544 (Medela AG, 2005) has gone furthest, with 93 descendants of its own.
How does its category compare?
All BTA devicesBTA Pump, Portable, Aspiration (Manual Or Powered): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · BTA
7so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · BTA
87in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · BTA
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · BTA
13in 2025
MAUDE reports naming product code BTA, 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 | 1 | — | 1 | 13 |
| 2008 | 3 | 135 | 3 | 5 |
| 2009 | 2 | — | 0 | 14 |
| 2010 | 2 | — | 3 | 178 |
| 2011 | 1 | — | 0 | 62 |
| 2012 | 1 | — | 0 | 47 |
| 2013 | 3 | 45 | 0 | 18 |
| 2014 | 3 | 91 | 0 | 399 |
| 2015 | 0 | — | 0 | 15 |
| 2016 | 3 | 149 | 0 | 25 |
| 2017 | 1 | — | 0 | 4 |
| 2018 | 4 | 125 | 0 | 17 |
| 2019 | 0 | — | 0 | 14 |
| 2020 | 1 | — | 0 | 10 |
| 2021 | 1 | — | 1 | 9 |
| 2022 | 3 | 58 | 0 | 7 |
| 2023 | 4 | 265 | 0 | 8 |
| 2024 | 5 | 131 | 0 | 13 |
| 2025 | 6 | 87 | 0 | 13 |
| 2026 | 7 | 89 | 0 | — |
https://510kreport.com/device/K933902 · printed Nov 6, 2026
Cite this page
510(k) Report. “K933902: Moblvac Iii.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K933902
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026