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FDA 510(k)

SERVO GAS MONITOR 120

K-Number: K861625 · 1986-05-02

ApplicantSiemens Elema AB
Decision Date1986-05-02
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO GAS MONITOR 120 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Elema AB. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861625. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO GAS MONITOR 120?

SERVO GAS MONITOR 120 is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Siemens Elema AB. The 510(k) number is K861625.

When did SERVO GAS MONITOR 120 receive FDA 510(k) clearance?

SERVO GAS MONITOR 120 received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861625.

Who is the listed applicant for SERVO GAS MONITOR 120?

The FDA 510(k) record lists Siemens Elema AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERVO GAS MONITOR 120?

The FDA product code for SERVO GAS MONITOR 120 is CCL.

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Other records listing Siemens Elema AB 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.

K023354COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EK010923KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392EK010925SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407EK002137CATHCOR DESKTOPK001315MODIFICATION TO KION ANESTHESIA SYSTEMK970839SERVO VENTILATOR 300A

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Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, Inc.

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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