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FDA 510(k)

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION

K-Number: K051634 · 2005-07-19

ApplicantGE Healthcare
Decision Date2005-07-19
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2005-07-19 under 510(k) number K051634. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION?

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION is a medical device that received FDA 510(k) clearance on 2005-07-19. The listed applicant is GE Healthcare. The 510(k) number is K051634.

When did DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION receive FDA 510(k) clearance?

DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION received FDA 510(k) clearance on 2005-07-19, under 510(k) number K051634.

Who is the listed applicant for DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION?

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

What is the FDA product code for DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION?

The FDA product code for DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION is MSX.

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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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