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)

ANESTHETIC AGENT MONITOR

K-Number: K892854 · 1989-10-13

ApplicantCriticare Systems, Inc.
Decision Date1989-10-13
Product CodeCBQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHETIC AGENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Criticare Systems, Inc.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K892854. 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 ANESTHETIC AGENT MONITOR?

ANESTHETIC AGENT MONITOR is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Criticare Systems, Inc.. The 510(k) number is K892854.

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

ANESTHETIC AGENT MONITOR received FDA 510(k) clearance on 1989-10-13, under 510(k) number K892854.

Who is the listed applicant for ANESTHETIC AGENT MONITOR?

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

What is the FDA product code for ANESTHETIC AGENT MONITOR?

The FDA product code for ANESTHETIC 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 Criticare Systems, 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.

K101602VITAL SIGNS MONITORK091050506CN PATIENT MONITORK0425698600 VITAL SIGNS MONITORK030613VITAL SIGNS MONITOR W/ARRHYTHMIA DETECTION AND ST ANALYSIS, MODEL 8100K022435507EL VITAL SIGNS MONITORK0120598100/8500 VITAL SIGNS MONITOR

View all 22 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.

↑