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FDA 510(k)

INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR

K-Number: K983250 · 1999-12-12

ApplicantMagnetic Resonance Equipment Corp.
Decision Date1999-12-12
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Magnetic Resonance Equipment Corp.. It received FDA 510(k) clearance on 1999-12-12 under 510(k) number K983250. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR?

INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR is a medical device that received FDA 510(k) clearance on 1999-12-12. The listed applicant is Magnetic Resonance Equipment Corp.. The 510(k) number is K983250.

When did INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR receive FDA 510(k) clearance?

INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR received FDA 510(k) clearance on 1999-12-12, under 510(k) number K983250.

Who is the listed applicant for INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR?

The FDA 510(k) record lists Magnetic Resonance Equipment Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR?

The FDA product code for INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR is DSK.

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.

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Other records listing Magnetic Resonance Equipment Corp. 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.

K003982TEMPERATURE FUNCTION, MODEL 9500 MULTIGAS MONITORK954120MODEL 9500 MR-COMPATIBLE MULTIGAS MONITORK924285MODEL 3500 MR-COMPATIBLE PULSE OXIMETERK924282MODEL 320 MR-COMPATIBLE PULSE OXIMETER

Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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