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)

ICOR AGENT MONITOR

K-Number: K883532 · 1988-11-04

ApplicantIcor AB
Decision Date1988-11-04
Product CodeCBQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ICOR AGENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Icor AB. It received FDA 510(k) clearance on 1988-11-04 under 510(k) number K883532. The device is classified under product code CBQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICOR AGENT MONITOR?

ICOR AGENT MONITOR is a medical device that received FDA 510(k) clearance on 1988-11-04. The listed applicant is Icor AB. The 510(k) number is K883532.

When did ICOR AGENT MONITOR receive FDA 510(k) clearance?

ICOR AGENT MONITOR received FDA 510(k) clearance on 1988-11-04, under 510(k) number K883532.

Who is the listed applicant for ICOR AGENT MONITOR?

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

What is the FDA product code for ICOR AGENT MONITOR?

The FDA product code for ICOR AGENT MONITOR is CBQ.

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 Icor AB 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.

K954402ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K953507TYPE 1 & 2 (HUMIDAIR I & II)K952325ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K952823FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBEK941987HEAT AND MOISTURE EXCHANGERS AND FILTERSK940041COLIBRI

View all 16 devices →

Related Devices (Code: CBQ)

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.

K040917PHILIPS ANESTHESIA GAS MONITOR, MODEL M1026BPhilips Medizin Systeme Boeblingen GmbHK994188MODIFICATION TO AGILENT TECHNOLOGIES ANESTHESIA GAS MONITOR, MODEL M1026A #CO5Agilent Technologies, GmbHK962648OHMEDA MODEL 5330 ANESTHETIC AGENT MONITOROhmeda MedicalK931439OHMEDA MODEL 5330 ANESTHETIC MONITOROhmeda MedicalK926451DATASCOPE MULTINEX IIDatascope Corp.K923433AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULEInstrumentarium Corp.

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.

↑