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FDA 510(k)

CAPNOMAC ULTIMA ANESTHESIA MONITOR

K-Number: K932098 · 1993-11-29

ApplicantDatex Division Instrumentarium Corp.
Decision Date1993-11-29
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPNOMAC ULTIMA ANESTHESIA 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 1993-11-29 under 510(k) number K932098. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPNOMAC ULTIMA ANESTHESIA MONITOR?

CAPNOMAC ULTIMA ANESTHESIA MONITOR is a medical device that received FDA 510(k) clearance on 1993-11-29. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K932098.

When did CAPNOMAC ULTIMA ANESTHESIA MONITOR receive FDA 510(k) clearance?

CAPNOMAC ULTIMA ANESTHESIA MONITOR received FDA 510(k) clearance on 1993-11-29, under 510(k) number K932098.

Who is the listed applicant for CAPNOMAC ULTIMA ANESTHESIA MONITOR?

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

What is the FDA product code for CAPNOMAC ULTIMA ANESTHESIA MONITOR?

The FDA product code for CAPNOMAC ULTIMA ANESTHESIA MONITOR is BZK.

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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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Related Devices (Code: BZK)

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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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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