510(k) · Cleared
ClearedAnapnoGuard 100 Respiratory Guard System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hospitech Respiration, Ltd. · BSK Cuff, Tracheal Tube, Inflatable
Cleared on Feb 16, 2016 as substantially equivalent to K092733 (Arm Medical Devices, Inc., 2010) and 2 other predicates after a 389-day review. Its family tree reaches back 6 generations to 1995. 4 of the 35 devices in its family, counting itself, have a Class I recall. 2 later devices descend from it.
- Decided
- Feb 16, 2016
- Review
- 389 days
- Class
- Class II
- Product code
- BSK
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 6 generations to K945062 (1995). 32 ancestors in all, the oldest K791045 (1979). 2 later devices descend from it, 1 citing it directly. 4 of the 35 devices in this family, counting this one, have a Class I recall.
- Root · 6 generations backK945062 VacplusKinetic Concepts, Inc. · 1995
- 5 generations backK971548 AmbuvacKinetic Concepts, Inc. · 1997
- 4 generations backK032310 Mini V.a.C., V.a.C. Freedom, V.a.C. AtsKinetic Concepts, Inc. · 2003 · Recalled
- 3 generations backK080357 Medela Invia Wound TherapyMedela AG · 2008 · Recalled
- 2 generations backK113291 Simex Negative Pressure Wound Therapy Powered Suction Pumps Series…Simex Medizintechnik GmbH · 2012
- 1 generation backK141255 Simex Subglottic Aspiration SystemSimex Medizintechnik GmbH · 2014
- This deviceK150157 AnapnoGuard 100 Respiratory Guard SystemHospitech Respiration, Ltd. · 2016
- Descendant · cites it directly · 1 of its ownK180991 AG 100sHospitech Respiration, Ltd. · 2018
- Descendant · 2 generations on · 0 of its ownK221477 AG100sHospitech Respiration, Ltd. · 2022
Class I recalls in this family
- K993786 Rusch Oral/Nasal (Safety Clear Plus) Tracheal…3 generations back · 2000
- K961837 Rush Oral/Nasal Tracheal Tube Cuffed Magill/Murphy3 generations back · 1996
- K961840 Rusch Oral/Nasal Tracheal Tube, Plain…3 generations back · 1996
- K931163 Rusch Agt PVC Preform Oral Trach Tub/Cuf W/Mur Eye3 generations back · 1993
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K945062 | Vacplus | Kinetic Concepts, Inc. | 1995 | — |
| −5 | K971548 | Ambuvac | Kinetic Concepts, Inc. | 1997 | — |
| −4 | K032310 | Mini V.a.C., V.a.C. Freedom, V.a.C. Ats | Kinetic Concepts, Inc. | 2003 | 2 |
| −3 | K080357 | Medela Invia Wound Therapy | Medela AG | 2008 | 1 |
| −2 | K113291 | Simex Negative Pressure Wound Therapy Powered Suction Pumps Series: Sim-EX200… | Simex Medizintechnik GmbH | 2012 | — |
| −1 | K141255 | Simex Subglottic Aspiration System | Simex Medizintechnik GmbH | 2014 | — |
| 0 (this device) | K150157 | AnapnoGuard 100 Respiratory Guard System | Hospitech Respiration, Ltd. | 2016 | — |
| +1 | K180991 | AG 100s | Hospitech Respiration, Ltd. | 2018 | — |
| +2 | K221477 | AG100s | Hospitech Respiration, Ltd. | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1987 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 1 | 0 |
| 1993 | 1 | 1 |
| 1994 | 1 | 0 |
| 1995 | 1 | 0 |
| 1996 | 2 | 2 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 2 | 1 |
| 2002 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 2 | 0 |
| 2006 | 3 | 0 |
| 2008 | 2 | 0 |
| 2010 | 2 | 0 |
| 2012 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 1 | 0 |
| 2022 | 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.
4 devices in this family have a Class I recall. 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 BSK device
- #1 K261499 TrachFlushscore 13.0 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K092733 | PYTONSummary page 6…valence to the following predicate devices is claimed: Device Name 510k No Clearance Date PYTON Cuff Pressure K092733 Feb 26, 2010 Regulator SIMEX subglottic K141255 September 22, 2014 A… | 2010 |
| * | K141255 | Simex Subglottic Aspiration SystemSummary page 6…510k No Clearance Date PYTON Cuff Pressure K092733 Feb 26, 2010 Regulator SIMEX subglottic K141255 September 22, 2014 Aspiration System (suction) Hospitech Respiration AnapnoGuard Endot… | 2014 |
| * | K093126 | Anapnoguard Endotracheal TubeSummary page 4…following three main components: The AnapnoGuard endotracheal tube (ETT) with inflatable cuff (FDA cleared under K093126). The AnapnoGuard 100 Respiratory Guard System interconnection harness of tu… | 2010 |
| † | K082520 | Sealguard Evac Endotracheal and Endotracheal Tubes | 2008 |
| † | K091761 | Teleflex Isis HVT Tracheal Tube, Cuffed, with Subglottic Secretion Suction Port | 2009 |
| † | K031997 | Mallinckrodt Dar TY-Care / TY-Care Exel Closed Suction System | 2003 |
| † | K081805 | Cuffalert | 2008 |
| † | K081778 | NS Series Vacuum/Pressure Gauges, Cuff Pressure Monitors | 2008 |
| † | K024300 | Microcap Plus/NPB-75 | 2003 |
| † | K103803 | Hamilton-G5 | 2011 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K180991 | AG 100s | 2018 | 1 |
Has anything in its family been recalled? (4 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K993786Rusch Oral/Nasal (Safety Clear Plus) Tracheal Tube Cuffed, Magill/MurphyRusch Intl. · 2000 · 3 generations back · ◆ in the 2000 ancestors bar of FIG. 13 Class I recalls
- K961837Rush Oral/Nasal Tracheal Tube Cuffed Magill/MurphyRusch Intl. · 1996 · 3 generations back · ◆ in the 1996 ancestors bar of FIG. 132 Class I recalls
- K961840Rusch Oral/Nasal Tracheal Tube, Plain Magill/MurphyRusch Intl. · 1996 · 3 generations back · ◆ in the 1996 ancestors bar of FIG. 124 Class I recalls
- K931163Rusch Agt PVC Preform Oral Trach Tub/Cuf W/Mur EyeRusch, Inc. · 1993 · 3 generations back · ◆ in the 1993 ancestors bar of FIG. 112 Class I recalls
What does this lineage say?
- The line of descent spans 21 years and passes through 4 companies; a new generation was cleared every 4.1 years on median.
- 13 of the 32 ancestors have a recall of any class; 4 have a Class I recall.
- Of its descendants, K180991 (Hospitech Respiration, Ltd., 2018) has gone furthest, with 1 descendant of its own.
- 4 other devices also cite its predicate K092733.
How does its category compare?
All BSK devicesBSK Cuff, Tracheal Tube, Inflatable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · BSK
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · BSK
376in 2016
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · BSK
1in 2017
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · BSK
46in 2025
MAUDE reports naming product code BSK, 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 | 2 |
| 2009 | 0 | — | 0 | 3 |
| 2010 | 1 | — | 0 | 5 |
| 2011 | 3 | 171 | 0 | 15 |
| 2012 | 2 | — | 0 | 62 |
| 2013 | 1 | — | 1 (1) | 16 |
| 2014 | 0 | — | 0 | 5 |
| 2015 | 1 | — | 0 | 1 |
| 2016 | 4 | 376 | 0 | 1 |
| 2017 | 0 | — | 1 | 3 |
| 2018 | 2 | — | 0 | 4 |
| 2019 | 1 | — | 0 | 2 |
| 2020 | 2 | — | 0 | 1 |
| 2021 | 1 | — | 0 | 9 |
| 2022 | 1 | — | 0 | 4 |
| 2023 | 1 | — | 0 | 51 |
| 2024 | 0 | — | 0 | 133 |
| 2025 | 2 | — | 0 | 46 |
| 2026 | 1 | — | 1 | — |
What is it indicated for?
AnapnoGuard 100 Respiratory Guard System is intended for airway management by oral/nasal intubation while providing continuous endotracheal cuff pressure control using non-invasive measurement and monitoring of carbon dioxide concentration in the subglottic space and evacuation of secretions from above the endotracheal tube’s cuff.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K150157 · printed Nov 6, 2026
Cite this page
510(k) Report. “K150157: AnapnoGuard 100 Respiratory Guard System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K150157
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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