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FDA 510(k)

SIREMOBIL CO2

K-Number: K973598 · 1997-11-10

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1997-11-10
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIREMOBIL CO2 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1997-11-10 under 510(k) number K973598. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIREMOBIL CO2?

SIREMOBIL CO2 is a medical device that received FDA 510(k) clearance on 1997-11-10. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K973598.

When did SIREMOBIL CO2 receive FDA 510(k) clearance?

SIREMOBIL CO2 received FDA 510(k) clearance on 1997-11-10, under 510(k) number K973598.

Who is the listed applicant for SIREMOBIL CO2?

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

What is the FDA product code for SIREMOBIL CO2?

The FDA product code for SIREMOBIL CO2 is OXO.

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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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