FDA 510(k)

MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM

K-Number: K122539 · 2013-04-19

Decision Date2013-04-19

Product CodeCHL

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics. It received FDA 510(k) clearance on 2013-04-19 under 510(k) number K122539. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM?

MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM is a medical device that received FDA 510(k) clearance on 2013-04-19. The listed applicant is Siemens Healthcare Diagnostics. The 510(k) number is K122539.

When did MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM receive FDA 510(k) clearance?

MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM received FDA 510(k) clearance on 2013-04-19, under 510(k) number K122539.

Who is the listed applicant for MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM?

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

What is the FDA product code for MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM?

The FDA product code for MEASUREMENT OF PH IN PLEURAL FLUID ON BLOOD GAS SYSTEM is CHL.

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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.