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FDA 510(k)

SmartSpectra Vital Signs Monitor 1.0

K-Number: K254169 · 2026-06-18

ApplicantPresage Security, Inc. d/b/a Presage Technologies, Inc.
Decision Date2026-06-18
Product CodeQME
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SmartSpectra Vital Signs Monitor 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Presage Security, Inc. d/b/a Presage Technologies, Inc.. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K254169. The device is classified under product code QME. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SmartSpectra Vital Signs Monitor 1.0?

SmartSpectra Vital Signs Monitor 1.0 is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Presage Security, Inc. d/b/a Presage Technologies, Inc.. The 510(k) number is K254169.

When did SmartSpectra Vital Signs Monitor 1.0 receive FDA 510(k) clearance?

SmartSpectra Vital Signs Monitor 1.0 received FDA 510(k) clearance on 2026-06-18, under 510(k) number K254169.

Who is the listed applicant for SmartSpectra Vital Signs Monitor 1.0?

The FDA 510(k) record lists Presage Security, Inc. d/b/a Presage Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SmartSpectra Vital Signs Monitor 1.0?

The FDA product code for SmartSpectra Vital Signs Monitor 1.0 is QME.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT04011163Vital Signs-Integrated Patient-Assisted Intravenous Opioid Analgesia for Post Surgical PainACTIVE_NOT_RECRUITINGNCT06238180Personalised Real-time Interoperable Sepsis Monitoring (PRISM)WITHDRAWNNCT06693817Advanced Wireless Sensors for Neonatal Care in the Delivery RoomRECRUITINGNCT06942338Comparative Evaluation of Body Temperature Measurement Using the CardioWatch 287-2 in an Intensive Care Setting.NOT_YET_RECRUITINGNCT07231653Home Monitoring Study for Surgical PatientsNOT_YET_RECRUITINGNCT07496346Integration of a Robotic Platform for Clinical Monitoring of Patients With Severe Acquired Brain Injury in High-Intensity Care UnitsNOT_YET_RECRUITING

Related Devices (Code: QME)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253650Anura Mobile Core SDK (M1)Nuralogix CorporationK260066PanopticAI Vital Signs (1.6.1-22)PanopticAI Technologies LimitedK251200Vital SignsOxehealth LimitedK243687Vital SignsOxehealth LimitedK250078Informed Vital Core Application (IVC App) (v2.0.0.2.0.0)Mindset Medical, Inc.K240890PanopticAI Vital SignsPanopticAI technologies Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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