510(k) · Cleared
Recalled · 2007Spacelabs Medical Multiparameter Module 91496
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Spacelabs Medical, Inc. · DSI Detector And Alarm, Arrhythmia
Cleared on May 3, 2005 as substantially equivalent to K050175 (Spacelabs Medical, Inc., 2005) and 2 other predicates after a 54-day review. Its family tree reaches back 6 generations to 1997. 1 later device descends from it. It has been recalled once.
- Decided
- May 3, 2005
- Review
- 54 days
- Class
- Class II
- Product code
- DSI
- Recalls
- 1
- Predicates
- 3
Its longest line of descent runs back 6 generations to K962603 (1997). 25 ancestors in all, the oldest K882609 (1989). 1 later device descends from it, 1 citing it directly.
- Root · 6 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
- 5 generations backK973887 Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and…Masimo Corp. · 1998
- 4 generations backK982255 Model 2000 Pulse OximeterIvy Biomedical Systems, Inc. · 1998
- 3 generations backK991823 N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc. · 1999
- 2 generations backK012891 Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax…Nellcor Puritan Bennett, Inc. · 2002 · Recalled
- 1 generation backK050175 Spacelabs Medical Multiparameter Module 91496Spacelabs Medical, Inc. · 2005
- This deviceK050605 Spacelabs Medical Multiparameter Module 91496Spacelabs Medical, Inc. · 2005
- Descendant · cites it directly · 0 of its ownK103142 Spacelabs Multi-Parameter ModuleSpacelabs Healthcare, Inc. · 2011 · Recalled
Most influential descendants
Showing 1 of 1 · See all- K103142Spacelabs Multi-Parameter ModuleSpacelabs Healthcare, Inc. · 2011 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K962603 | Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & Cables | Masimo Corp. | 1997 | — |
| −5 | K973887 | Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and Cables | Masimo Corp. | 1998 | — |
| −4 | K982255 | Model 2000 Pulse Oximeter | Ivy Biomedical Systems, Inc. | 1998 | — |
| −3 | K991823 | N-395 Pulse Oximeter, Model N-395 | Nellcor Puritan Bennett, Inc. | 1999 | — |
| −2 | K012891 | Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax Sensors and… | Nellcor Puritan Bennett, Inc. | 2002 | 1 |
| −1 | K050175 | Spacelabs Medical Multiparameter Module 91496 | Spacelabs Medical, Inc. | 2005 | — |
| 0 (this device) | K050605 | Spacelabs Medical Multiparameter Module 91496 | Spacelabs Medical, Inc. | 2005 | — |
| +1 | K103142 | Spacelabs Multi-Parameter Module | Spacelabs Healthcare, Inc. | 2011 | 14 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1989 | 1 | 0 |
| 1990 | 3 | 0 |
| 1991 | 1 | 0 |
| 1994 | 3 | 0 |
| 1995 | 3 | 0 |
| 1996 | 1 | 0 |
| 1997 | 2 | 0 |
| 1998 | 1 | 0 |
| 1999 | 1 | 0 |
| 2000 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 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.
Planning a device in DSI? 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 DSI device
- #1 K243349 BodyGuardian Remote Monitoring System (BGRMS…score 13.1 · 9 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 |
|---|---|---|---|
| * | K050175 | Spacelabs Medical Multiparameter Module 91496 Our reading of the summary gave K051175, FDA’s number for Civ-OB Obstrical Monitoring Software Application (Civent Communications, Ltd.), decided Feb 17, 2006, after this device. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Spacelabs Medical Integrated Multiparameter Module 91496 with Option…”. | 2005 |
| * | K972502 | Spacelabs Medical Integrated Multiparameter Module 90496Summary page 1…K051175: Spacelabs Medical Integrated Multiparameter Module 91496 with Option N Devices: (Nellcor SP0 2 oximetry) K972502: Spacelabs Medical Integrated Multiparameter Module 90496 K033296: Masimo Corp. SET Rad-5 Pulse Oximeter… | 1998 |
| * | K033296 | Masimo Set Rad-5 Pulse Oximeter, Model Rad-5; Masimo Set Rad-5V Pulse Oximeter, Model…Summary page 1…on N Devices: (Nellcor SP0 2 oximetry) K972502: Spacelabs Medical Integrated Multiparameter Module 90496 K033296: Masimo Corp. SET Rad-5 Pulse Oximeter… | 2004 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K103142 | Spacelabs Multi-Parameter Module | 2011 | 0 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 3, 2007 | Not classified | Z-0523-2007 | Other | Potential for modules to reset, alarms returning to default settings, invasive pressure losing its labels and zero calibration and Sp02 alarm limits being frozen. This can result in delay in treatment. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 8 years and passes through 4 companies; a new generation was cleared every 11 months on median.
- 6 of the 25 ancestors have a recall of any class.
- Of its descendants, K103142 (Spacelabs Healthcare, Inc., 2011) has gone furthest, with 0 descendants of its own.
How does its category compare?
All DSI devicesDSI Detector And Alarm, Arrhythmia: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DSI
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DSI
243in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DSI
18in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DSI
712in 2025
MAUDE reports naming product code DSI, 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 | 7 | 151 | 4 | 64 |
| 2008 | 5 | 70 | 8 | 156 |
| 2009 | 6 | 73 | 3 | 279 |
| 2010 | 6 | 111 | 5 | 823 |
| 2011 | 6 | 114 | 3 | 793 |
| 2012 | 3 | 113 | 1 | 766 |
| 2013 | 1 | — | 0 | 795 |
| 2014 | 4 | 200 | 0 | 1,000 |
| 2015 | 9 | 127 | 0 | 1,645 |
| 2016 | 6 | 224 | 0 | 4,352 |
| 2017 | 0 | — | 0 | 3,594 |
| 2018 | 2 | — | 1 | 3,648 |
| 2019 | 3 | 243 | 4 | 3,485 |
| 2020 | 2 | — | 2 | 3,084 |
| 2021 | 0 | — | 0 | 3,092 |
| 2022 | 0 | — | 1 | 1,638 |
| 2023 | 2 | — | 2 | 1,616 |
| 2024 | 1 | — | 0 | 1,320 |
| 2025 | 1 | — | 18 | 712 |
| 2026 | 1 | — | 1 | — |
What is it indicated for?
Conditions to be screened, monitored, treated or diagnosed. Patient conditions indicated by abnormalities in various physiologic parameters, including ECG waveform, respiratory effort, invasive and noninvasive blood pressure measurements, temperature, cardiac output, and pulse oximeter (SpO2) readings. Specific to the physiologic parameter being monitored, accessories may be applied externally to the chest and limbs or invasively into the blood stream.…
Read the full statement (227 words)
Conditions to be screened, monitored, treated or diagnosed.
Patient conditions indicated by abnormalities in various physiologic parameters, including ECG waveform, respiratory effort, invasive and noninvasive blood pressure measurements, temperature, cardiac output, and pulse oximeter (SpO2) readings.
Specific to the physiologic parameter being monitored, accessories may be applied externally to the chest and limbs or invasively into the blood stream.
Frequency as directed by physician.
In conjunction with clinical findings, a screening and diagnostic tool for use in:
assessing electrical activity of the heart in order to detect abnormal cardiac rhythms, including life threatening events such as high and low heart rates, asystole and ventricular fibrillation as well as, in adults, the detection of rhythms such as ventricular runs, tachycardia, and ST segment deviations;
monitoring respiratory effort to detect abnormal respiration events such as high and low respiration rates and episodes of apnea;
continuous monitoring of invasive pressure signals to detect abnormal events such as high and low pressure;
episodic monitoring of noninvasive pressure signals to detect abnormal events such as high and low pressure;
continuous monitoring of temperature signals to detect abnormal events such as high and low body temperature;
monitoring of the patient's pumping ability of the heart and various hemodynamic values to detect abnormal flow volumes; and
noninvasive, continuous monitoring of pulse oxygen saturation signals in order to detect desaturation due to abnormal pulmonary/circulatory functions.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K050605 · printed Nov 6, 2026
Cite this page
510(k) Report. “K050605: Spacelabs Medical Multiparameter Module 91496.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050605
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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