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)

OHMEDA MODEL 5330 ANESTHETIC MONITOR

K-Number: K931439 · 1993-10-19

ApplicantOhmeda Medical
Decision Date1993-10-19
Product CodeCBQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA MODEL 5330 ANESTHETIC MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1993-10-19 under 510(k) number K931439. 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 OHMEDA MODEL 5330 ANESTHETIC MONITOR?

OHMEDA MODEL 5330 ANESTHETIC MONITOR is a medical device that received FDA 510(k) clearance on 1993-10-19. The listed applicant is Ohmeda Medical. The 510(k) number is K931439.

When did OHMEDA MODEL 5330 ANESTHETIC MONITOR receive FDA 510(k) clearance?

OHMEDA MODEL 5330 ANESTHETIC MONITOR received FDA 510(k) clearance on 1993-10-19, under 510(k) number K931439.

Who is the listed applicant for OHMEDA MODEL 5330 ANESTHETIC MONITOR?

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

What is the FDA product code for OHMEDA MODEL 5330 ANESTHETIC MONITOR?

The FDA product code for OHMEDA MODEL 5330 ANESTHETIC 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 Ohmeda Medical 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.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

View all 119 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 MedicalK926451DATASCOPE MULTINEX IIDatascope Corp.K923433AS/3 ANAESTHESIA MONITORING SYSTEM AIRWAY MODULEInstrumentarium Corp.K922876AS/3 COP MODULEDatex Division Instrumentarium 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.

↑