510(k) Report

510(k) · Cleared

Cleared

SOMAVAC 100 Sustained Vacuum System

K222856510(k) SpecialCleared Oct 19, 202228-day reviewClass II21 CFR 878.4780

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Somavac Medical Solutions, Inc. · BTA Pump, Portable, Aspiration (Manual Or Powered)

Cleared on Oct 19, 2022 as substantially equivalent to K180606 (Somavac Medical Solutions, Inc., 2018) after a 28-day review. Its family tree reaches back 3 generations to 1988. 2 later devices descend from it.

Decided
Oct 19, 2022
Review
28 days
Class
Class II
Product code
BTA
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K883582 (1988). 5 ancestors in all. 2 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2014: 1 other ancestor1998: 1 other ancestor2023: 2 descendants clearedK883582 · Varidyne Model 250 Suction Drainage System · Surgidyne, Inc. · 1988K972703 · Redyrob-Closed Wound Drainage System · B.Braun Medical, Inc. · 1997K180606 · SOMAVAC Device · Somavac Medical Solutions, Inc. · 20181990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 2 descendants K180606 · SOMAVAC Device · Somavac Medical Solutions, Inc. · 2018K972703 · Redyrob-Closed Wound Drainage System · B.Braun Medical, Inc. · 1997K883582 · Varidyne Model 250 Suction Drainage System · Surgidyne, Inc. · 19880
  1. Root · 3 generations backK883582 Varidyne Model 250 Suction Drainage SystemSurgidyne, Inc. · 1988
  2. 2 generations backK972703 Redyrob-Closed Wound Drainage SystemB.Braun Medical, Inc. · 1997
  3. 1 generation backK180606 SOMAVAC DeviceSomavac Medical Solutions, Inc. · 2018
  4. This deviceK222856 SOMAVAC 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc. · 2022
  5. Descendant · cites it directly · 0 of its ownK231063 SOMAVAC® 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc. · 2023
  6. Descendant · cites it directly · 0 of its ownK223373 Enivo™Aroa Biosurgery, Ltd. · 2023

Most influential descendants

Showing 2 of 2 · See all
  • K231063SOMAVAC® 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc. · 2023 · cites it directly0descendants
  • K223373Enivo™Aroa Biosurgery, Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K883582Varidyne Model 250 Suction Drainage SystemSurgidyne, Inc.1988—
−2K972703Redyrob-Closed Wound Drainage SystemB.Braun Medical, Inc.1997—
−1K180606SOMAVAC DeviceSomavac Medical Solutions, Inc.2018—
0 (this device)K222856SOMAVAC 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc.2022—
+1K231063SOMAVAC® 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc.2023—
+1K223373Enivo™Aroa Biosurgery, Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202320
FIG. 1 — Lineage of K222856, 1988–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 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. #1 K222547 Electric nasal aspiratorscore 20.7 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K180606SOMAVAC Device
Summary page 4
…ification: Class II Regulation Number: 21 CFR 878.4780 Panel: General and Plastic Surgery Product Code: BTA Primary Predicate: SOMAVAC® Device (K180606), Manufacturer: SOMAVAC Medical Solutions, Inc.…
Somavac Medical Solutions, Inc.2018—

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K231063SOMAVAC® 100 Sustained Vacuum SystemSomavac Medical Solutions, Inc.20230
K223373Enivo™Aroa Biosurgery, Ltd.20230

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 34 years and passes through 3 companies; a new generation was cleared every 9.0 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K231063 (Somavac Medical Solutions, Inc., 2023) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BTA devices

BTA Pump, Portable, Aspiration (Manual Or Powered): FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · BTA

7so far in 2026, the most since 2007

2007: 12008: 32009: 22010: 22011: 12012: 12013: 32014: 32016: 32017: 12018: 42020: 12021: 12022: 32023: 42024: 52025: 62026 (partial year): 7
2007high 7 (2026) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BTA

87in 2025

2008: 135 days median2013: 45 days median2014: 91 days median2016: 149 days median2018: 125 days median2022: 58 days median2023: 265 days median2024: 131 days median2025: 87 days median2026 (partial year): 89 days median
2007high 265 (2023) · low 45 (2013)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · BTA

1in 2021

2007: 12008: 32010: 32021: 1
2007high 3 (2008) · low 0 (2009)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · BTA

13in 2025

2007: 132008: 52009: 142010: 1782011: 622012: 472013: 182014: 3992015: 152016: 252017: 42018: 172019: 142020: 102021: 92022: 72023: 82024: 132025: 13
2007high 399 (2014) · low 4 (2017)2025

MAUDE reports naming product code BTA, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—113
2008313535
20092—014
20102—3178
20111—062
20121—047
2013345018
20143910399
20150—015
20163149025
20171—04
20184125017
20190—014
20201—010
20211—19
202235807
2023426508
20245131013
2025687013
20267890—

What is it indicated for?

The SOMAVAC® 100 Sustained Vacuum System (SOMAVAC® 100) is a portable battery powered vacuum source / waste container intended for the removal of surgical and bodily fluids from a closed wound following plastic surgery and other general surgery forming large flaps for hematoma and seroma prophylaxis. It is intended for use in homecare and healthcare environments.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K222856: SOMAVAC 100 Sustained Vacuum System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K222856

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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