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FDA 510(k)

NORMAC ANESTHETIC AGENT MONITOR

K-Number: K832113 · 1983-09-12

ApplicantDatex Division Instrumentarium Corp.
Decision Date1983-09-12
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NORMAC ANESTHETIC AGENT 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 1983-09-12 under 510(k) number K832113. The device is classified under product code CBS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORMAC ANESTHETIC AGENT MONITOR?

NORMAC ANESTHETIC AGENT MONITOR is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K832113.

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

NORMAC ANESTHETIC AGENT MONITOR received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832113.

Who is the listed applicant for NORMAC ANESTHETIC AGENT 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 NORMAC ANESTHETIC AGENT MONITOR?

The FDA product code for NORMAC ANESTHETIC AGENT MONITOR is CBS.

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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: CBS)

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.

K974903GAS MODULE II, MODEL 0998-00-0143Datascope Corp.K953795VITALMAX 4100Pace Tech, Inc.K960490AS/3 COMPACT AIRWAY MODULE M-CAIOVDatex Medical Instrumentation, Inc.K951366RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18)Riken Keiki Co., Ltd.K950101RAMS (RANDOM ACCESS MASS SPECTROMETER) M-200 RESPIRATORY GAS MONITORMarquette Electronics, Inc.K943458AS/3 AIRWAY 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.

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