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)

JDM SP2 SENSOR

K-Number: K873806 · 1987-12-08

ApplicantJd Monitoring C/O Mackler, Cooper and Gibbs
Decision Date1987-12-08
Product CodeKMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JDM SP2 SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Jd Monitoring C/O Mackler, Cooper and Gibbs. It received FDA 510(k) clearance on 1987-12-08 under 510(k) number K873806. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JDM SP2 SENSOR?

JDM SP2 SENSOR is a medical device that received FDA 510(k) clearance on 1987-12-08. The listed applicant is Jd Monitoring C/O Mackler, Cooper and Gibbs. The 510(k) number is K873806.

When did JDM SP2 SENSOR receive FDA 510(k) clearance?

JDM SP2 SENSOR received FDA 510(k) clearance on 1987-12-08, under 510(k) number K873806.

Who is the listed applicant for JDM SP2 SENSOR?

The FDA 510(k) record lists Jd Monitoring C/O Mackler, Cooper and Gibbs as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JDM SP2 SENSOR?

The FDA product code for JDM SP2 SENSOR is KMI.

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

Related Devices (Code: KMI)

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.

K131585INTEL-GE CARE INNOVATIONS QUIETCAREIntel-Ge Care Innovations, LLCK130752DYNASENSE SYSTEMCentauri Medical, Inc.K101109VIVATRAKWireless Medcare, LLCK090138MOBILECARE MONITOR, MODEL 2100Aframe Digital, Inc.K942770ULTIMAT-SENSOR FOR BED OCCUPANCY MONITORUltimate Development Corp.K943481INFORMER PLUSMicro-Tech 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.

↑