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FDA 510(k)

MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR

K-Number: K861707 · 1986-06-19

ApplicantSiemens Elema AB
Decision Date1986-06-19
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR 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 1986-06-19 under 510(k) number K861707. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR?

MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Siemens Elema AB. The 510(k) number is K861707.

When did MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR receive FDA 510(k) clearance?

MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR received FDA 510(k) clearance on 1986-06-19, under 510(k) number K861707.

Who is the listed applicant for MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR?

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 MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR?

The FDA product code for MASTER PROGRAM FLOW & PRESSURE CO2 & LUNG MONITOR is CBK.

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Related Devices (Code: CBK)

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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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