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FDA 510(k)

SPECTRAMED RESPIRATORY GAS ANALYZER

K-Number: K873194 · 1987-10-30

ApplicantDraeger Medical, Inc.
Decision Date1987-10-30
Product CodeCBS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SPECTRAMED RESPIRATORY GAS ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1987-10-30 under 510(k) number K873194. 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 SPECTRAMED RESPIRATORY GAS ANALYZER?

SPECTRAMED RESPIRATORY GAS ANALYZER is a medical device that received FDA 510(k) clearance on 1987-10-30. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K873194.

When did SPECTRAMED RESPIRATORY GAS ANALYZER receive FDA 510(k) clearance?

SPECTRAMED RESPIRATORY GAS ANALYZER received FDA 510(k) clearance on 1987-10-30, under 510(k) number K873194.

Who is the listed applicant for SPECTRAMED RESPIRATORY GAS ANALYZER?

The FDA 510(k) record lists Draeger Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTRAMED RESPIRATORY GAS ANALYZER?

The FDA product code for SPECTRAMED RESPIRATORY GAS ANALYZER is CBS.

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Other records listing Draeger Medical, 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.

K042607PRIMUS USK042419FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEMK042276D-VAPORK042086FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK041622MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEMK040847MODIFICATION TO VAMOS ANESTHETIC GAS 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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