Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SENSOCOR(TM) R-TEST 240 XL

K-Number: K881772 · 1988-11-09

ApplicantSensormedix, Inc.
Decision Date1988-11-09
Product CodeDXH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SENSOCOR(TM) R-TEST 240 XL is the device name listed in this FDA 510(k) record. The listed applicant is Sensormedix, Inc.. It received FDA 510(k) clearance on 1988-11-09 under 510(k) number K881772. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOCOR(TM) R-TEST 240 XL?

SENSOCOR(TM) R-TEST 240 XL is a medical device that received FDA 510(k) clearance on 1988-11-09. The listed applicant is Sensormedix, Inc.. The 510(k) number is K881772.

When did SENSOCOR(TM) R-TEST 240 XL receive FDA 510(k) clearance?

SENSOCOR(TM) R-TEST 240 XL received FDA 510(k) clearance on 1988-11-09, under 510(k) number K881772.

Who is the listed applicant for SENSOCOR(TM) R-TEST 240 XL?

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

What is the FDA product code for SENSOCOR(TM) R-TEST 240 XL?

The FDA product code for SENSOCOR(TM) R-TEST 240 XL is DXH. This falls under the Hematology category.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sensormedix, Inc. 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.

K881771SENSOCOR(TM) DIASYS

Related Devices (Code: DXH)

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.

K250233PreemptiveAI Clinical SDKMeasure Labs, Inc. (Dba Preemptiveai, Inc.)K250258HeartBeam AIMIGo with 12-L ECG Synthesis Software SystemHeartbeam, Inc.K243438MEMO Patch M (MPT-E08R-UNC01)Huinno Co., Ltd.K243981Hexoskin Medical System (7100-00016)Carre Technologies, Inc.K243003VitalSigns 1-Lead Holter (VSH101)VitalSigns Technology Co., Ltd.K233521QT ECG (QTERD100)QT Medical, 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.

↑