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FDA 510(k)

SIEMENS FIO2 SENSOR

K-Number: K991884 · 1999-11-03

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1999-11-03
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS FIO2 SENSOR 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 1999-11-03 under 510(k) number K991884. 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 SIEMENS FIO2 SENSOR?

SIEMENS FIO2 SENSOR is a medical device that received FDA 510(k) clearance on 1999-11-03. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K991884.

When did SIEMENS FIO2 SENSOR receive FDA 510(k) clearance?

SIEMENS FIO2 SENSOR received FDA 510(k) clearance on 1999-11-03, under 510(k) number K991884.

Who is the listed applicant for SIEMENS FIO2 SENSOR?

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 SIEMENS FIO2 SENSOR?

The FDA product code for SIEMENS FIO2 SENSOR is CCL.

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Related Devices (Code: CCL)

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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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