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FDA 510(k)

ABM ANESTHESIA & BRAIN MONITOR

K-Number: K840232 · 1984-04-06

ApplicantDatex Division Instrumentarium Corp.
Decision Date1984-04-06
Product Code
DecisionSubstantially Equivalent

Device Summary

ABM ANESTHESIA & BRAIN MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Datex Division Instrumentarium Corp.. It received FDA 510(k) clearance on 1984-04-06 under 510(k) number K840232. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABM ANESTHESIA & BRAIN MONITOR?

ABM ANESTHESIA & BRAIN MONITOR is a medical device that received FDA 510(k) clearance on 1984-04-06. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K840232.

When did ABM ANESTHESIA & BRAIN MONITOR receive FDA 510(k) clearance?

ABM ANESTHESIA & BRAIN MONITOR received FDA 510(k) clearance on 1984-04-06, under 510(k) number K840232.

Who is the listed applicant for ABM ANESTHESIA & BRAIN MONITOR?

The FDA 510(k) record lists Datex Division Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Datex Division Instrumentarium 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.

K953175AS/3 ESTPR MODULEK961247AS/3 LIGHT MONITORK943458AS/3 AIRWAY MODULEK945234AS/3 MEMORY MODULE, M0MEMK933156DATEX AS/3 PATIENT MONITORK933285DATEX AS/3 TM ANAESTHESIA MONITOR

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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.

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