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FDA 510(k)

Neteera 130H-Plus Vital Sign Monitoring Sensor

K-Number: K231733 · 2024-02-09

ApplicantNeteera Technologies , Ltd.
Decision Date2024-02-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Neteera 130H-Plus Vital Sign Monitoring Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Neteera Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-09 under 510(k) number K231733. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neteera 130H-Plus Vital Sign Monitoring Sensor?

Neteera 130H-Plus Vital Sign Monitoring Sensor is a medical device that received FDA 510(k) clearance on 2024-02-09. The listed applicant is Neteera Technologies , Ltd.. The 510(k) number is K231733.

When did Neteera 130H-Plus Vital Sign Monitoring Sensor receive FDA 510(k) clearance?

Neteera 130H-Plus Vital Sign Monitoring Sensor received FDA 510(k) clearance on 2024-02-09, under 510(k) number K231733.

Who is the listed applicant for Neteera 130H-Plus Vital Sign Monitoring Sensor?

The FDA 510(k) record lists Neteera Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Neteera 130H-Plus Vital Sign Monitoring Sensor?

The FDA product code for Neteera 130H-Plus Vital Sign Monitoring Sensor is DRT.

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.

NCT06232876Continuous Versus Intermittent Ward MonitoringNOT_YET_RECRUITINGNCT06693817Advanced Wireless Sensors for Neonatal Care in the Delivery RoomRECRUITINGNCT07105189Feasibility of Wireless Continuous Vital Sign Monitoring and Impact on Patients Undergoing Adult Spinal Surgery in a General WardRECRUITINGNCT07732257Wireless MicroPremVitals Button Sensor in the NICURECRUITINGNCT07739810Miniaturized Vital Sign Monitoring for Newborns in the Delivery RoomNOT_YET_RECRUITING

Other records listing Neteera Technologies , Ltd. as applicant

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.

K212143Neteera 130H/131H Vital Sign Monitoring Sensor

Related Devices (Code: DRT)

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.

K261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.K232354Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server SoftwareMurata Vios, Inc.

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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