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FDA 510(k)

SIEMENS-ELEMA AB CO2 MONITOR 130

K-Number: K802459 · 1980-10-23

ApplicantSiemens Elema AB
Decision Date1980-10-23
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS-ELEMA AB CO2 MONITOR 130 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 1980-10-23 under 510(k) number K802459. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS-ELEMA AB CO2 MONITOR 130?

SIEMENS-ELEMA AB CO2 MONITOR 130 is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Siemens Elema AB. The 510(k) number is K802459.

When did SIEMENS-ELEMA AB CO2 MONITOR 130 receive FDA 510(k) clearance?

SIEMENS-ELEMA AB CO2 MONITOR 130 received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802459.

Who is the listed applicant for SIEMENS-ELEMA AB CO2 MONITOR 130?

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 SIEMENS-ELEMA AB CO2 MONITOR 130?

The FDA product code for SIEMENS-ELEMA AB CO2 MONITOR 130 is CCK.

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Related Devices (Code: CCK)

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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