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FDA 510(k)

ANESTHETIC GAS MONITOR

K-Number: K890446 · 1989-08-11

ApplicantBruel & Kjaer Instruments, Inc.
Decision Date1989-08-11
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHETIC GAS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Bruel & Kjaer Instruments, Inc.. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K890446. 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 ANESTHETIC GAS MONITOR?

ANESTHETIC GAS MONITOR is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Bruel & Kjaer Instruments, Inc.. The 510(k) number is K890446.

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

ANESTHETIC GAS MONITOR received FDA 510(k) clearance on 1989-08-11, under 510(k) number K890446.

Who is the listed applicant for ANESTHETIC GAS MONITOR?

The FDA 510(k) record lists Bruel & Kjaer Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHETIC GAS MONITOR?

The FDA product code for ANESTHETIC GAS MONITOR is CBS.

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 Bruel & Kjaer Instruments, Inc. 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.

K901881VIBROMETRY SYSTEMK827409REAL TIME ULTRASOUND SCANNER 1849K827380SCANNER TYPE 1846

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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